A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608442



Internal ID16395851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:133734046..134166111hg38UCSC Ensembl
Innerchr7:133418799..133850863hg19UCSC Ensembl
Innerchr7:133069339..133501403hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38432066
hg19432065
hg18432065
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155234
SamplesHGDP00465
Known GenesEXOC4, LRGUK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608442
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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