A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7583



Internal ID15552607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122592545..122619520hg38UCSC Ensembl
Outerchr10:124352061..124379036hg19UCSC Ensembl
Outerchr10:124342051..124369026hg18UCSC Ensembl
Outerchr10:124342051..124369026hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg387854
hg197854
hg187854
hg177854
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5324
SamplesNA19129
Known GenesDMBT1
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)nsv7583
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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