A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655767



Internal ID18607362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29865090..29909182hg38UCSC Ensembl
Innerchr6:29832867..29876959hg19UCSC Ensembl
Innerchr6:29940846..29984938hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3844093
hg1944093
hg1844093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029680
Supporting Variants
Samples
Known GenesHLA-H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655767
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