A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575816



Internal ID16016539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60335320..60336225hg38UCSC Ensembl
Innerchr17:58412681..58413586hg19UCSC Ensembl
Innerchr17:55767463..55768368hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38906
hg19906
hg18906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5737n54
Supporting Variantsnssv875675, nssv875682, nssv875686, nssv875680, nssv875678, nssv875676, nssv875671, nssv875673, nssv875681, nssv875670, nssv875677, nssv875683, nssv875684, nssv875685, nssv875672, nssv875674, nssv875679, nssv875669, nssv875668
Samples
Known GenesUSP32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575816
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer