A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017359



Internal ID18759894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17384160..17459117hg38UCSC Ensembl
Innerchr6:17384391..17459348hg19UCSC Ensembl
Innerchr6:17492370..17567327hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3874958
hg1974958
hg1874958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5921n100
Supporting Variantsnssv3654805
Samples
Known GenesCAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017359
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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