A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7618



Internal ID15552645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:129929777..129961881hg38UCSC Ensembl
Outerchr10:131728041..131760145hg19UCSC Ensembl
Outerchr10:131618031..131650135hg18UCSC Ensembl
Outerchr10:131618031..131650135hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg387304
hg197304
hg187304
hg177304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6426
SamplesNA12156
Known GenesEBF3
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)nsv7618
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer