A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv816723



Internal ID16110679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85947860..85996277hg38UCSC Ensembl
Innerchr13:86521995..86570412hg19UCSC Ensembl
Innerchr13:85419996..85468413hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3848418
hg1948418
hg1848418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562611
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv816723
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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