A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8828



Internal ID15535036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:86463994..86497793hg38UCSC Ensembl
Outerchr10:88223751..88257550hg19UCSC Ensembl
Outerchr10:88213731..88247530hg18UCSC Ensembl
Outerchr10:88213731..88247530hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg385636
hg195636
hg185636
hg175636
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7478
Supporting Variants
SamplesNA12156
Known GenesWAPAL
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)nssv8828
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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