A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5558



Internal ID15543895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:54820575..54848660hg38UCSC Ensembl
Outerchr15:55112773..55140858hg19UCSC Ensembl
Outerchr15:52900065..52928150hg18UCSC Ensembl
Outerchr15:52900065..52928150hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3810522
hg1910522
hg1810522
hg1710522
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1540
Supporting Variants
SamplesNA19129
Known Genes
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)nssv5558
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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