A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1643



Internal ID15546206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:84570700..84605025hg38UCSC Ensembl
Outerchr15:85113931..85148256hg19UCSC Ensembl
Outerchr15:82914935..82949260hg18UCSC Ensembl
Outerchr15:82914935..82949260hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg385707
hg195707
hg185707
hg175707
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2941
SamplesNA18555
Known GenesLINC00933, UBE2Q2P1, ZSCAN2
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)nsv1643
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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