A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710221



Internal ID16004177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13111025..13151920hg38UCSC Ensembl
Innerchr1:13178497..13219371hg19UCSC Ensembl
Innerchr1:13101084..13141958hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3840896
hg1940875
hg1840875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545544
Supporting Variants
Samples
Known GenesHNRNPCP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710221
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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