A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4128



Internal ID15538855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:82028148..82044776hg38UCSC Ensembl
Outerchr14:82494492..82511120hg19UCSC Ensembl
Outerchr14:81564245..81580873hg18UCSC Ensembl
Outerchr14:81564245..81580873hg17UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3816629
hg1916629
hg1816629
hg1716629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1377
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)nssv4128
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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