A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699357



Internal ID15436009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:57552431..57622117hg38UCSC Ensembl
Innerchr1:58018103..58087789hg19UCSC Ensembl
Innerchr1:57790691..57860377hg18UCSC Ensembl
Innerchr1:57730124..57799810hg17UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3869687
hg1969687
hg1869687
hg1769687
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523574
Supporting Variants
Samples
Known GenesDAB1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699357
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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