A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1639



Internal ID15546202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:81977136..82010096hg38UCSC Ensembl
Outerchr15:82269477..82302437hg19UCSC Ensembl
Outerchr15:80056532..80089492hg18UCSC Ensembl
Outerchr15:80056532..80089492hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386773
hg196773
hg186773
hg176773
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4168
SamplesNA12878
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)nsv1639
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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