A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708639



Internal ID16002595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1979139..1979763hg38UCSC Ensembl
Innerchr1:1910578..1911202hg19UCSC Ensembl
Innerchr1:1900438..1901062hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38625
hg19625
hg18625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545043
Supporting Variants
Samples
Known GenesKIAA1751
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708639
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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