A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1062523



Internal ID15915709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64927615..64999166hg38UCSC Ensembl
Innerchr6:65637508..65709059hg19UCSC Ensembl
Innerchr6:65694229..65765780hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3871552
hg1971552
hg1871552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603407
Supporting Variants
Samples
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1062523
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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