A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1386



Internal ID15545949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:86071058..86116143hg38UCSC Ensembl
Outerchr14:86537402..86582487hg19UCSC Ensembl
Outerchr14:85607155..85652240hg18UCSC Ensembl
Outerchr14:85607155..85652240hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3845086
hg1945086
hg1845086
hg1745086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9227
SamplesNA12156
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)nsv1386
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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