A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704952



Internal ID15441604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34356230..34369357hg38UCSC Ensembl
Innerchr1:34821831..34834958hg19UCSC Ensembl
Innerchr1:34594418..34607545hg18UCSC Ensembl
Innerchr1:34490924..34504051hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3813128
hg1913128
hg1813128
hg1713128
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528365
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704952
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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