A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562711



Internal ID16350120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91348132..91349096hg38UCSC Ensembl
Innerchr13:92000386..92001350hg19UCSC Ensembl
Innerchr13:90798387..90799351hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38965
hg19965
hg18965
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3315n54
Supporting Variantsnssv817455, nssv817458, nssv817453, nssv817457, nssv817456, nssv817452, nssv817459, nssv817454
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562711
Frequency
Sample Size17421
Observed Gain6
Observed Loss2
Observed Complex0
Frequencyn/a


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