A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657669



Internal ID18955950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65119187..65200785hg38UCSC Ensembl
Innerchr6:65829080..65910678hg19UCSC Ensembl
Innerchr6:65885801..65967399hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3881599
hg1981599
hg1881599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017889
Supporting Variants
Samples
Known GenesEYS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657669
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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