A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075593



Internal ID15582093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163403832..163414458hg38UCSC Ensembl
Innerchr6:163824864..163835490hg19UCSC Ensembl
Innerchr6:163744854..163755480hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3810627
hg1910627
hg1810627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605193
Supporting Variants
Samples
Known GenesCAHM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075593
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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