A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703194



Internal ID15093160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:35902179..35914532hg38UCSC Ensembl
Innerchr1:36367780..36380133hg19UCSC Ensembl
Innerchr1:36140367..36152720hg18UCSC Ensembl
Innerchr1:36036873..36049226hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3812354
hg1912354
hg1812354
hg1712354
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526837
Supporting Variants
Samples
Known GenesAGO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703194
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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