A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5073



Internal ID15549846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:152172285..152217479hg38UCSC Ensembl
Outerchr5:151551846..151597040hg19UCSC Ensembl
Outerchr5:151532039..151577233hg18UCSC Ensembl
Outerchr5:151532039..151577233hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3845195
hg1945195
hg1845195
hg1745195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2555
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)nsv5073
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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