A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576031



Internal ID16016754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:75590683..75596271hg38UCSC Ensembl
Innerchr17:73586764..73592352hg19UCSC Ensembl
Innerchr17:71098359..71103947hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg385589
hg195589
hg185589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876107
Samples
Known GenesMYO15B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576031
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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