A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705937



Internal ID15095903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:162191130..162191212hg38UCSC Ensembl
Innerchr1:162160920..162161002hg19UCSC Ensembl
Innerchr1:160427544..160427626hg18UCSC Ensembl
Innerchr1:158892578..158892660hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3883
hg1983
hg1883
hg1783
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516482
Supporting Variants
Samples
Known GenesNOS1AP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705937
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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