A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574787



Internal ID16362196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36201388..36210694hg38UCSC Ensembl
Innerchr17:34528788..34538096hg19UCSC Ensembl
Innerchr17:31552901..31562209hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg389307
hg199309
hg189309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5544n54
Supporting Variantsnssv869922, nssv869925, nssv869921, nssv869926, nssv869924, nssv869923
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574787
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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