A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654731



Internal ID18953012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4255406..4473880hg38UCSC Ensembl
Innerchr6:4255640..4474114hg19UCSC Ensembl
Innerchr6:4200639..4419113hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38218475
hg19218475
hg18218475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020205
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)nssv3654731
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