A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574998



Internal ID16362407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40743159..40768780hg38UCSC Ensembl
Innerchr17:38899411..38925032hg19UCSC Ensembl
Innerchr17:36152937..36178558hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3825622
hg1925622
hg1825622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5589n54
Supporting Variantsnssv870539
Samples
Known GenesKRT25, KRT26
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574998
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