A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608482



Internal ID16395891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140175698..140176542hg38UCSC Ensembl
Innerchr7:139875498..139876342hg19UCSC Ensembl
Innerchr7:139521967..139522811hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38845
hg19845
hg18845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1094824, nssv1094822, nssv1094823
Samples
Known GenesKDM7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608482
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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