A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609160



Internal ID16396569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155346915..155350287hg38UCSC Ensembl
Innerchr7:155139614..155142990hg19UCSC Ensembl
Innerchr7:154832371..154835743hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg383373
hg193377
hg183373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1100352
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609160
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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