A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387



Internal ID15551291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37053048..37087575hg38UCSC Ensembl
Outerchr10:37341976..37376503hg19UCSC Ensembl
Outerchr10:37381982..37416509hg18UCSC Ensembl
Outerchr10:37381982..37416509hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg385494
hg195494
hg185494
hg175494
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2844
SamplesNA18555
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)nsv6387
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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