A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017934



Internal ID18760467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17391479..17448482hg38UCSC Ensembl
Innerchr6:17391710..17448713hg19UCSC Ensembl
Innerchr6:17499689..17556692hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3857004
hg1957004
hg1857004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5921n100
Supporting Variantsnssv3654807
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)nsv1017934
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer