A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031151



Internal ID18773684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17384160..17457369hg38UCSC Ensembl
Innerchr6:17384391..17457600hg19UCSC Ensembl
Innerchr6:17492370..17565579hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3873210
hg1973210
hg1873210
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5921n100
Supporting Variantsnssv3654804, nssv3654803
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)nsv1031151
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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