A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608063



Internal ID16395472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103160250..103166988hg38UCSC Ensembl
Innerchr7:102800697..102807435hg19UCSC Ensembl
Innerchr7:102587933..102594671hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg386739
hg196739
hg186739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11553n54
Supporting Variantsnssv1092072
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608063
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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