A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1076256



Internal ID15929442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165656355..165694678hg38UCSC Ensembl
Innerchr6:166069843..166108166hg19UCSC Ensembl
Innerchr6:165989833..166028156hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3838324
hg1938324
hg1838324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605254
Supporting Variants
Samples
Known GenesPDE10A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1076256
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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