A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576139



Internal ID16363548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:80489186..80524044hg38UCSC Ensembl
Innerchr17:78462986..78497844hg19UCSC Ensembl
Innerchr17:76077581..76112439hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3834859
hg1934859
hg1834859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876909
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576139
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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