A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1908



Internal ID15541191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103394163..103424722hg38UCSC Ensembl
Outerchr10:105153920..105184479hg19UCSC Ensembl
Outerchr10:105143910..105174469hg18UCSC Ensembl
Outerchr10:105143910..105174469hg17UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg389440
hg199440
hg189440
hg179440
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7529
Supporting Variants
SamplesNA18555
Known GenesMIR1307, PDCD11, USMG5
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)nssv1908
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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