A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649063



Internal ID18947344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94776661..94934177hg38UCSC Ensembl
Innerchr6:95486379..95643895hg19UCSC Ensembl
Innerchr6:95543100..95700616hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38157517
hg19157517
hg18157517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029987
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)nssv3649063
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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