A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606808



Internal ID16394217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44955728..44961683hg38UCSC Ensembl
Innerchr7:44995327..45001282hg19UCSC Ensembl
Innerchr7:44961852..44967807hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg385956
hg195956
hg185956
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1083558, nssv1083557
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606808
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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