A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609166



Internal ID16396575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156041367..156071994hg38UCSC Ensembl
Innerchr7:155834061..155864688hg19UCSC Ensembl
Innerchr7:155526822..155557449hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3830628
hg1930628
hg1830628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11753n54
Supporting Variantsnssv1155929
SamplesNINDS_61
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609166
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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