A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649865



Internal ID18948146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102250820..102288461hg38UCSC Ensembl
Innerchr6:102698695..102736336hg19UCSC Ensembl
Innerchr6:102805388..102843029hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3837642
hg1937642
hg1837642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017801
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)nssv3649865
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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