A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605982



Internal ID16393391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5093588..5183325hg38UCSC Ensembl
Innerchr7:5133219..5222956hg19UCSC Ensembl
Innerchr7:5099745..5189482hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3889738
hg1989738
hg1889738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078810
Samples
Known GenesZNF890P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605982
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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