A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022363



Internal ID19111581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160610658..160647652hg38UCSC Ensembl
Innerchr6:161031690..161068684hg19UCSC Ensembl
Innerchr6:160951680..160988674hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3836995
hg1936995
hg1836995
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6166n100
Supporting Variantsnssv3749570, nssv3654504
Samples
Known GenesLPA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022363
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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