A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3653087



Internal ID18951368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169354572..169390590hg38UCSC Ensembl
Innerchr6:169754667..169790685hg19UCSC Ensembl
Innerchr6:169496592..169532610hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3836019
hg1936019
hg1836019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031925
Supporting Variants
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)nssv3653087
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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