A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607719



Internal ID16395128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85752298..85887605hg38UCSC Ensembl
Innerchr7:85381614..85516921hg19UCSC Ensembl
Innerchr7:85219550..85354857hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38135308
hg19135308
hg18135308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1089379
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607719
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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