A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6642



Internal ID15190536
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 StatusS
Merged Variantsnsv1613
Supporting Variants
SamplesNA12156
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)nssv6642
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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