A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9512



Internal ID15193116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:34385772..34530514hg38UCSC Ensembl
Outerchr15:34677973..34822715hg19UCSC Ensembl
Outerchr15:32465265..32610007hg18UCSC Ensembl
Outerchr15:32465265..32610007hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38144743
hg19144743
hg18144743
hg17144743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1485
Supporting Variants
SamplesNA18507
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)nssv9512
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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