A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10332



Internal ID15195780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:183834..198035hg38UCSC Ensembl
Outerchr3:225517..239718hg19UCSC Ensembl
Outerchr3:200517..214718hg18UCSC Ensembl
Outerchr3:200517..214718hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3814202
hg1914202
hg1814202
hg1714202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3670
Supporting Variants
SamplesNA18956
Known GenesCHL1
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)nssv10332
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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