A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8837



Internal ID15535027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:101156925..101190052hg38UCSC Ensembl
Outerchr10:102916682..102949809hg19UCSC Ensembl
Outerchr10:102906672..102939799hg18UCSC Ensembl
Outerchr10:102906672..102939799hg17UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg386312
hg196312
hg186312
hg176312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7526
Supporting Variants
SamplesNA12156
Known Genes
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)nssv8837
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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