A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155418



Internal ID22085923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41257158..41274279hg38UCSC Ensembl
Outerchr17:41251729..41276472hg38UCSC Ensembl
Innerchr17:39413410..39430531hg19UCSC Ensembl
Outerchr17:39407981..39432724hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3824744
hg1924744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010514, nssv4010513
Samples
Known GenesKRTAP9-6, KRTAP9-7, KRTAP9-9
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155418
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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