A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4115



Internal ID15538842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:58747063..58755708hg38UCSC Ensembl
Outerchr14:59213781..59222426hg19UCSC Ensembl
Outerchr14:58283534..58292179hg18UCSC Ensembl
Outerchr14:58283534..58292179hg17UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg385397
hg195397
hg185397
hg175397
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1291
Supporting Variants
SamplesNA12878
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)nssv4115
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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