A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1100317



Internal ID15953503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155345856..155350553hg38UCSC Ensembl
Innerchr7:155138556..155143184hg19UCSC Ensembl
Innerchr7:154831312..154836009hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384698
hg194629
hg184698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609143
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)nssv1100317
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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