A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561215



Internal ID16001938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19871303..20076371hg38UCSC Ensembl
Innerchr13:20445443..20650511hg19UCSC Ensembl
Innerchr13:19343443..19548511hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38205069
hg19205069
hg18205069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806053
Samples
Known GenesZMYM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561215
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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