A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576193



Internal ID16016916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82226048..82237706hg38UCSC Ensembl
Innerchr17:80183924..80195582hg19UCSC Ensembl
Innerchr17:77777213..77788871hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3811659
hg1911659
hg1811659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877126
Samples
Known GenesMIR6787, SLC16A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576193
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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