A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1061734



Internal ID15914920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64236276..64271007hg38UCSC Ensembl
Innerchr6:64946169..64980900hg19UCSC Ensembl
Innerchr6:65004128..65038859hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3834732
hg1934732
hg1834732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603389
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)nssv1061734
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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