A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6625



Internal ID15190553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:34419641..34601539hg38UCSC Ensembl
Outerchr15:34711842..34893740hg19UCSC Ensembl
Outerchr15:32499134..32681032hg18UCSC Ensembl
Outerchr15:32499134..32681032hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38181899
hg19181899
hg18181899
hg17181899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1485
Supporting Variants
SamplesNA12156
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
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)nssv6625
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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