A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2455



Internal ID15540674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:18132027..18176743hg38UCSC Ensembl
Outerchr4:18133650..18178366hg19UCSC Ensembl
Outerchr4:17742748..17787464hg18UCSC Ensembl
Outerchr4:17809919..17854635hg17UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3844717
hg1944717
hg1844717
hg1744717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4257
Supporting Variants
SamplesNA18555
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)nssv2455
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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