A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704581



Internal ID15441233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:167034302..167040846hg38UCSC Ensembl
Innerchr1:167003539..167010083hg19UCSC Ensembl
Innerchr1:165270163..165276707hg18UCSC Ensembl
Innerchr1:163735197..163741741hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg386545
hg196545
hg186545
hg176545
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528049
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704581
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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