A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1246



Internal ID15197794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:34354006..34543415hg38UCSC Ensembl
Outerchr15:34646207..34835616hg19UCSC Ensembl
Outerchr15:32433499..32622908hg18UCSC Ensembl
Outerchr15:32433499..32622908hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38189410
hg19189410
hg18189410
hg17189410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1485
Supporting Variants
SamplesNA19240
Known GenesGOLGA8A, GOLGA8B, LPCAT4, MIR1233-1, MIR1233-2, NUTM1
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)nssv1246
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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