A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817453



Internal ID16111409
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 loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562711
Supporting Variants
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817453
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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