A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698064



Internal ID15088030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14501818..14514303hg38UCSC Ensembl
Innerchr3:14543326..14555811hg19UCSC Ensembl
Innerchr3:14518330..14530815hg18UCSC Ensembl
Innerchr3:14518330..14530815hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3812486
hg1912486
hg1812486
hg1712486
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521453
Supporting Variants
Samples
Known GenesGRIP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698064
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer