A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561213



Internal ID16001936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19828738..19900631hg38UCSC Ensembl
Innerchr13:20402878..20474771hg19UCSC Ensembl
Innerchr13:19300878..19372771hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3871894
hg1971894
hg1871894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806051
Samples
Known GenesZMYM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561213
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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