A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710901



Internal ID15658171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16898769..16932783hg38UCSC Ensembl
Innerchr1:17225264..17259278hg19UCSC Ensembl
Innerchr1:17097851..17131865hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3834015
hg1934015
hg1834015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545676
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)nssv710901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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