A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6776



Internal ID15551719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:57079407..57110743hg38UCSC Ensembl
Outerchr10:58839167..58870503hg19UCSC Ensembl
Outerchr10:58509173..58540509hg18UCSC Ensembl
Outerchr10:58509173..58540509hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3831337
hg1931337
hg1831337
hg1731337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1896
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)nsv6776
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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