A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074596



Internal ID15927782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152554727..152605382hg38UCSC Ensembl
Innerchr6:152875862..152926517hg19UCSC Ensembl
Innerchr6:152917555..152968210hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3850656
hg1950656
hg1850656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604912
Supporting Variants
Samples
Known GenesSYNE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1074596
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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