A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545541



Internal ID15986264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13075113..13151495hg38UCSC Ensembl
Innerchr1:13137578..13218946hg19UCSC Ensembl
Innerchr1:13060165..13141533hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3876383
hg1981369
hg1881369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv710218
Samples
Known GenesHNRNPCP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545541
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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