A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1906



Internal ID15194503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:95786879..95820014hg38UCSC Ensembl
Outerchr10:97546636..97579771hg19UCSC Ensembl
Outerchr10:97536626..97569761hg18UCSC Ensembl
Outerchr10:97536626..97569761hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg386893
hg196893
hg186893
hg176893
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7500
Supporting Variants
SamplesNA18555
Known GenesENTPD1, ENTPD1-AS1
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)nssv1906
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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