A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607731



Internal ID16048454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88037351..88042993hg38UCSC Ensembl
Innerchr7:87666666..87672308hg19UCSC Ensembl
Innerchr7:87504602..87510244hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg385643
hg195643
hg185643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1089392, nssv1089390, nssv1089391
Samples
Known GenesADAM22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607731
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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