A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034230



Internal ID18776764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64869168..65177857hg38UCSC Ensembl
Innerchr6:65579061..65887750hg19UCSC Ensembl
Innerchr6:65635782..65944471hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38308690
hg19308690
hg18308690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657653
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)nsv1034230
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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