A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402



Internal ID15204622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:133043596..133072827hg38UCSC Ensembl
Outerchr8:134055841..134085072hg19UCSC Ensembl
Outerchr8:134125023..134154254hg18UCSC Ensembl
Outerchr8:134125023..134154254hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3810276
hg1910276
hg1810276
hg1710276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10643
SamplesNA18956
Known GenesMIR7848, SLA, TG
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)nsv6402
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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