A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607308



Internal ID16394717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64105575..64323008hg38UCSC Ensembl
Innerchr7:63565953..63783386hg19UCSC Ensembl
Innerchr7:63203388..63420821hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38217434
hg19217434
hg18217434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11415n54
Supporting Variantsnssv1085470, nssv1085469, nssv1085468
Samples
Known GenesZNF679, ZNF735, ZNF736
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607308
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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