A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6654



Internal ID15551585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:50262130..50291854hg38UCSC Ensembl
Outerchr10:52021890..52051614hg19UCSC Ensembl
Outerchr10:51691896..51721620hg18UCSC Ensembl
Outerchr10:51691896..51721620hg17UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg389768
hg199768
hg189768
hg179768
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10759
SamplesNA18956
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)nsv6654
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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