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dbVar

Database of genomic structural variation

nsv5615201

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert 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: 121 SVs from 23 studies. See in: genome view

Submitted genomic185,228,632-185,228,632

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5615201	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	185,228,632	185,228,632
nsv5615201	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	184,946,420	184,946,420

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17131617	insertion	HG01505	Sequencing	Sequence alignment	1,109

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17131617	Submitted genomic		NC_000003.12:g.185 228632_185228633in s999	GRCh38 (hg38)		NC_000003.12	Chr3	185,228,632	185,228,632
nssv17131617	Remapped	Perfect	NC_000003.11:g.184 946420_184946421in s999	GRCh37.p13	First Pass	NC_000003.11	Chr3	184,946,420	184,946,420

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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