A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562709



Internal ID16350118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91348005..91349096hg38UCSC Ensembl
Innerchr13:92000259..92001350hg19UCSC Ensembl
Innerchr13:90798260..90799351hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381092
hg191092
hg181092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3317n54
Supporting Variantsnssv817449
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562709
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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