A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705538



Internal ID15442190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:150701208..150703007hg38UCSC Ensembl
Innerchr1:150673684..150675483hg19UCSC Ensembl
Innerchr1:148940308..148942107hg18UCSC Ensembl
Innerchr1:147486757..147488556hg17UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg381800
hg191800
hg181800
hg171800
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528859
Supporting Variants
Samples
Known GenesHORMAD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705538
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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