A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4868



Internal ID15549620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:68002335..68027432hg38UCSC Ensembl
Outerchr5:67298163..67323260hg19UCSC Ensembl
Outerchr5:67333919..67359016hg18UCSC Ensembl
Outerchr5:67333919..67359016hg17UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3825098
hg1925098
hg1825098
hg1725098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8110
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)nsv4868
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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