A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1264



Internal ID15197774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:75253787..75294637hg38UCSC Ensembl
Outerchr15:75546128..75586978hg19UCSC Ensembl
Outerchr15:73333181..73374031hg18UCSC Ensembl
Outerchr15:73333181..73374031hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3840851
hg1940851
hg1840851
hg1740851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1613
Supporting Variants
SamplesNA19240
Known GenesGOLGA6C, GOLGA6D
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv1264
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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