A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576025



Internal ID16016748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:74778036..74818437hg38UCSC Ensembl
Innerchr17:72774175..72814576hg19UCSC Ensembl
Innerchr17:70285770..70326171hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3840402
hg1940402
hg1840402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149806
SamplesHGDP00402
Known GenesTMEM104
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576025
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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