A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv806772



Internal ID16100728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:24556367..24609927hg38UCSC Ensembl
Innerchr13:25130505..25184065hg19UCSC Ensembl
Innerchr13:24028505..24082065hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3853561
hg1953561
hg1853561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561344
Supporting Variants
Samples
Known GenesTPTE2P6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv806772
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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