A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608493



Internal ID16395902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140175929..140177015hg38UCSC Ensembl
Innerchr7:139875729..139876815hg19UCSC Ensembl
Innerchr7:139522198..139523284hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381087
hg191087
hg181087
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11624n54
Supporting Variantsnssv1094839
Samples
Known GenesKDM7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608493
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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