A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5559



Internal ID15543894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:59468853..59500554hg38UCSC Ensembl
Outerchr15:59761052..59792753hg19UCSC Ensembl
Outerchr15:57548344..57580045hg18UCSC Ensembl
Outerchr15:57548344..57580045hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg387557
hg197557
hg187557
hg177557
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1552
Supporting Variants
SamplesNA19129
Known GenesFAM81A
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)nssv5559
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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