A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4257



Internal ID15548948
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 StatusM
Merged Variants
Supporting Variantsnssv2455
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)nsv4257
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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