A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576138



Internal ID16363547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:80488563..80493611hg38UCSC Ensembl
Innerchr17:78462363..78467411hg19UCSC Ensembl
Innerchr17:76076958..76082006hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg385049
hg195049
hg185049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876907, nssv876908
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576138
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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