A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7530



Internal ID15552549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103627238..103658302hg38UCSC Ensembl
Outerchr10:105386995..105418060hg19UCSC Ensembl
Outerchr10:105376985..105408050hg18UCSC Ensembl
Outerchr10:105376985..105408050hg17UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg388364
hg198364
hg188364
hg178364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6412
SamplesNA12156
Known GenesSH3PXD2A
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)nsv7530
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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