A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6698



Internal ID15551633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:54270363..54314812hg38UCSC Ensembl
Outerchr10:56030123..56074572hg19UCSC Ensembl
Outerchr10:55700129..55744578hg18UCSC Ensembl
Outerchr10:55700129..55744578hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3844450
hg1944450
hg1844450
hg1744450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1895
SamplesNA18555
Known GenesPCDH15
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)nsv6698
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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