A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710915



Internal ID15658185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16919140..16935243hg38UCSC Ensembl
Innerchr1:17245635..17261738hg19UCSC Ensembl
Innerchr1:17118222..17134325hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3816104
hg1916104
hg1816104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545686
Supporting Variants
Samples
Known GenesCROCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710915
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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