A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1443



Internal ID15546006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105671362..106647801hg38UCSC Ensembl
Outerchr14:106137699..107103804hg19UCSC Ensembl
Outerchr14:105208744..106174849hg18UCSC Ensembl
Outerchr14:105208744..106174849hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38976440
hg19966106
hg18966106
hg17966106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10038, nssv4134, nssv1224, nssv6619, nssv9303, nssv10034, nssv1225, nssv6615, nssv2089, nssv5531, nssv2090, nssv10035, nssv4137, nssv10921, nssv4135, nssv5530, nssv6616, nssv1231, nssv9508, nssv9509, nssv5532, nssv1226, nssv2092
SamplesNA18507, NA12156, NA12878, NA18956, NA15510, NA18555, NA18517, NA19240, NA19129
Known GenesADAM6, ELK2AP, KIAA0125, LINC00221, LINC00226
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)nsv1443
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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