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dbVar

Database of genomic structural variation

nsv4768290

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Quan et al. 2021

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 324 SVs from 44 studies. See in: genome view

Remapped(Score: Perfect):879,374-879,374

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4768290	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	879,374	879,374
nsv4768290	Remapped	Perfect	GRCh38.p12	ALT_REF_LOCI_1	Second Pass	NT_187622.1	Chr19\|NT_1 87622.1	59,727	59,727
nsv4768290	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	879,374	879,374

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16273967	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16273967	Remapped	Perfect	NT_187622.1:g.5972 7_59728ins337	GRCh38.p12	Second Pass	NT_187622.1	Chr19\|NT_1 87622.1	59,727	59,727
nssv16273967	Remapped	Perfect	NC_000019.10:g.879 374_879375ins337	GRCh38.p12	First Pass	NC_000019.10	Chr19	879,374	879,374
nssv16273967	Submitted genomic		NC_000019.9:g.8793 74_879375ins337	GRCh37 (hg19)		NC_000019.9	Chr19	879,374	879,374

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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