A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606898



Internal ID16394307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50059808..50066137hg38UCSC Ensembl
Innerchr7:50099404..50105733hg19UCSC Ensembl
Innerchr7:50069950..50076279hg18UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg386330
hg196330
hg186330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1083838
Samples
Known GenesZPBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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