A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv819900



Internal ID16113856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110914065..110915734hg38UCSC Ensembl
Innerchr13:111566412..111568081hg19UCSC Ensembl
Innerchr13:110364413..110366082hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381670
hg191670
hg181670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563154
Supporting Variants
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv819900
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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