A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4108



Internal ID15538835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:40137602..40149516hg38UCSC Ensembl
Outerchr14:40606806..40618720hg19UCSC Ensembl
Outerchr14:39676557..39688471hg18UCSC Ensembl
Outerchr14:39676557..39688471hg17UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3811915
hg1911915
hg1811915
hg1711915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1249
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)nssv4108
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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