A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607862



Internal ID16395271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95391290..95395591hg38UCSC Ensembl
Innerchr7:95020602..95024903hg19UCSC Ensembl
Innerchr7:94858538..94862839hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384302
hg194302
hg184302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1091195
Samples
Known GenesPON3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607862
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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