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dbVar

Database of genomic structural variation

nsv4360648

Organism: Homo sapiens

Study:nstd169 (Giner-Delgado et al. 2019)
Variant Type:inversion
Method Type:MLPA
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:4,110

Publication(s):Giner-Delgado et al. 2019

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: 141 SVs from 40 studies. See in: genome view

Remapped(Score: Perfect):130,527,041-130,531,150

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4360648	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	130,527,041	130,531,150
nsv4360648	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000006.11	Chr6	130,848,186	130,852,295

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15607179	inversion	MLPA	Genotyping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15607179	Remapped	Perfect	NC_000006.12:g.130 527041_130531150in v	GRCh38.p12	First Pass	NC_000006.12	Chr6	130,527,041	130,531,150
nssv15607179	Submitted genomic		NC_000006.11:g.130 848186_130852295in v	GRCh37.p13		NC_000006.11	Chr6	130,848,186	130,852,295

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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