A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607788



Internal ID16395197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90504613..90589032hg38UCSC Ensembl
Innerchr7:90133927..90218346hg19UCSC Ensembl
Innerchr7:89971863..90056282hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3884420
hg1984420
hg1884420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155362
SamplesHGDP00956
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607788
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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