A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606342



Internal ID16047065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16875904..17375160hg38UCSC Ensembl
Innerchr7:16915528..17414784hg19UCSC Ensembl
Innerchr7:16882053..17381309hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38499257
hg19499257
hg18499257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11225n54
Supporting Variantsnssv1079632, nssv1079633, nssv1155306
SamplesHGDP01376
Known GenesAGR3, AHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606342
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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