A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3906



Internal ID15538633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:127785934..127821377hg38UCSC Ensembl
Outerchr10:129584198..129619641hg19UCSC Ensembl
Outerchr10:129474188..129509631hg18UCSC Ensembl
Outerchr10:129474188..129509631hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg384282
hg194282
hg184282
hg174282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7608
Supporting Variants
SamplesNA12878
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)nssv3906
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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