A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3338



Internal ID15538066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:26761581..26806425hg38UCSC Ensembl
Outerchr5:26761690..26806534hg19UCSC Ensembl
Outerchr5:26797447..26842291hg18UCSC Ensembl
Outerchr5:26797447..26842291hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3844845
hg1944845
hg1844845
hg1744845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4768
Supporting Variants
SamplesNA12878
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)nssv3338
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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