A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574917



Internal ID16362326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36780473..36788426hg38UCSC Ensembl
Innerchr17:35137651..35145634hg19UCSC Ensembl
Innerchr17:32211764..32219747hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387954
hg197984
hg187984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv870154
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574917
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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