A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710918



Internal ID15658188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16919140..16935719hg38UCSC Ensembl
Innerchr1:17245635..17262214hg19UCSC Ensembl
Innerchr1:17118222..17134801hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3816580
hg1916580
hg1816580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545687
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)nssv710918
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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