A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607306



Internal ID16394715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64065485..64300703hg38UCSC Ensembl
Innerchr7:63525863..63761081hg19UCSC Ensembl
Innerchr7:63163298..63398516hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38235219
hg19235219
hg18235219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11415n54
Supporting Variantsnssv1085466
Samples
Known GenesZNF679, ZNF727, ZNF735
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607306
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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