A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820688



Internal ID15767958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113812448..113820249hg38UCSC Ensembl
Innerchr13:114515421..114523222hg19UCSC Ensembl
Innerchr13:113590721..113598522hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg387802
hg197802
hg187802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563394
Supporting Variants
Samples
Known GenesGAS6-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv820688
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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