A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5548



Internal ID15197223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:34409540..34573063hg38UCSC Ensembl
Outerchr15:34701741..34865264hg19UCSC Ensembl
Outerchr15:32489033..32652556hg18UCSC Ensembl
Outerchr15:32489033..32652556hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38163524
hg19163524
hg18163524
hg17163524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1485
Supporting Variants
SamplesNA19129
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)nssv5548
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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