A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701556



Internal ID15091522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:35776427..35860595hg38UCSC Ensembl
Innerchr1:36242028..36326196hg19UCSC Ensembl
Innerchr1:36014615..36098783hg18UCSC Ensembl
Innerchr1:35911121..35995289hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3884169
hg1984169
hg1884169
hg1784169
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525430
Supporting Variants
Samples
Known GenesAGO4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701556
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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