A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609120



Internal ID16396529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155181214..155187164hg38UCSC Ensembl
Innerchr7:154972924..154978874hg19UCSC Ensembl
Innerchr7:154603857..154609807hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg385951
hg195951
hg185951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155927
SamplesHGDP01053
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609120
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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