A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7608



Internal ID15552634
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 StatusM
Merged Variants
Supporting Variantsnssv3906
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)nsv7608
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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