A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608426



Internal ID16395835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131947549..132020385hg38UCSC Ensembl
Innerchr7:131632308..131705144hg19UCSC Ensembl
Innerchr7:131282848..131355684hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3872837
hg1972837
hg1872837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155231
Samples1798860372_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608426
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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