A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574765



Internal ID16362174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36116419..36154379hg38UCSC Ensembl
Innerchr17:34443811..34481759hg19UCSC Ensembl
Innerchr17:31467924..31505872hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3837961
hg1937949
hg1837949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5535n54
Supporting Variantsnssv869877, nssv869876, nssv869887, nssv869880, nssv869888, nssv869882, nssv869886, nssv869885, nssv869889, nssv869884, nssv869879, nssv869878, nssv869881, nssv869883, nssv869875
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574765
Frequency
Sample Size17421
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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