A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6631



Internal ID15190547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:47209701..47220118hg38UCSC Ensembl
Outerchr15:47501898..47512315hg19UCSC Ensembl
Outerchr15:45289190..45299607hg18UCSC Ensembl
Outerchr15:45289190..45299607hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3810224
hg1910224
hg1810224
hg1710224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1526
Supporting Variants
SamplesNA12156
Known GenesSEMA6D
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)nssv6631
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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