A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6606



Internal ID15537257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:84824758..84863903hg38UCSC Ensembl
Outerchr14:85291102..85330247hg19UCSC Ensembl
Outerchr14:84360855..84400000hg18UCSC Ensembl
Outerchr14:84360855..84400000hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3839146
hg1939146
hg1839146
hg1739146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1383
Supporting Variants
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)nssv6606
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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