A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678149



Internal ID15414801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:122284910..122287680hg38UCSC Ensembl
Innerchr3:122003757..122006527hg19UCSC Ensembl
Innerchr3:123486447..123489217hg18UCSC Ensembl
Innerchr3:123486447..123489217hg17UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg382771
hg192771
hg182771
hg172771
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517368
Supporting Variants
Samples
Known GenesCASR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678149
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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