A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5101



Internal ID15549877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:161746821..161791672hg38UCSC Ensembl
Outerchr5:161173827..161218678hg19UCSC Ensembl
Outerchr5:161106405..161151256hg18UCSC Ensembl
Outerchr5:161106405..161151256hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3844852
hg1944852
hg1844852
hg1744852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8181
SamplesNA12156
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)nsv5101
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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