A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690632



Internal ID15427284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176171442..176197346hg38UCSC Ensembl
Innerchr3:175889230..175915134hg19UCSC Ensembl
Innerchr3:177371924..177397828hg18UCSC Ensembl
Innerchr3:177371932..177397836hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3825905
hg1925905
hg1825905
hg1725905
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516429
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690632
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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