A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4315



Internal ID15549012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:44035532..44081552hg38UCSC Ensembl
Outerchr4:44037549..44083569hg19UCSC Ensembl
Outerchr4:43732306..43778326hg18UCSC Ensembl
Outerchr4:43878477..43924497hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3846021
hg1946021
hg1846021
hg1746021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4738
SamplesNA19129
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)nsv4315
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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