A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017997



Internal ID18760530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26681681..26855769hg38UCSC Ensembl
Innerchr6:26681909..26823548hg19UCSC Ensembl
Innerchr6:26789888..26931527hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38174089
hg19141640
hg18141640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5929n100
Supporting Variantsnssv3654861
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017997
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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