A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498



Internal ID15204727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:42481130..42514602hg38UCSC Ensembl
Outerchr10:42976578..43010050hg19UCSC Ensembl
Outerchr10:42296584..42330056hg18UCSC Ensembl
Outerchr10:42296584..42330056hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg386558
hg196558
hg186558
hg176558
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2845
SamplesNA18555
Known GenesLINC00839, ZNF37BP
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)nsv6498
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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