A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4790



Internal ID15202849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:35090643..35123530hg38UCSC Ensembl
Outerchr5:35090745..35123632hg19UCSC Ensembl
Outerchr5:35126502..35159389hg18UCSC Ensembl
Outerchr5:35126502..35159389hg17UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3832888
hg1932888
hg1832888
hg1732888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8091
SamplesNA12156
Known GenesPRLR
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)nsv4790
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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