A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574443



Internal ID16361852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15280310..15281519hg38UCSC Ensembl
Innerchr17:15183627..15184836hg19UCSC Ensembl
Innerchr17:15124352..15125561hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381210
hg191210
hg181210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5464n54
Supporting Variantsnssv868377, nssv868376, nssv868375, nssv868374, nssv868378
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574443
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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