A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1613



Internal ID15199490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:75250491..75296314hg38UCSC Ensembl
Outerchr15:75542832..75588655hg19UCSC Ensembl
Outerchr15:73329885..73375708hg18UCSC Ensembl
Outerchr15:73329885..73375708hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3845824
hg1945824
hg1845824
hg1745824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6642, nssv1264
SamplesNA12156, NA19240
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)nsv1613
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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