A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704704



Internal ID15094670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:20589208..20608303hg38UCSC Ensembl
Innerchr1:20915701..20934796hg19UCSC Ensembl
Innerchr1:20788288..20807383hg18UCSC Ensembl
Innerchr1:20661007..20680102hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3819096
hg1919096
hg1819096
hg1719096
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528156
Supporting Variants
Samples
Known GenesCDA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704704
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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