A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1231



Internal ID15544497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:106410341..106465908hg38UCSC Ensembl
Outerchr14:106866254..106921833hg19UCSC Ensembl
Outerchr14:105937299..105992878hg18UCSC Ensembl
Outerchr14:105937299..105992878hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3855568
hg1955580
hg1855580
hg1755580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA19240
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)nssv1231
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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