A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606341



Internal ID16393750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16875904..17366094hg38UCSC Ensembl
Innerchr7:16915528..17405718hg19UCSC Ensembl
Innerchr7:16882053..17372243hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38490191
hg19490191
hg18490191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11225n54
Supporting Variantsnssv1079631, nssv1079630
Samples
Known GenesAGR3, AHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606341
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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