A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574786



Internal ID16362195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36201388..36209441hg38UCSC Ensembl
Innerchr17:34528788..34536843hg19UCSC Ensembl
Innerchr17:31552901..31560956hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg388054
hg198056
hg188056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5544n54
Supporting Variantsnssv869919, nssv869920
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574786
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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