A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3765



Internal ID15201721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:37756008..37801260hg38UCSC Ensembl
Outerchr3:37797499..37842751hg19UCSC Ensembl
Outerchr3:37772503..37817755hg18UCSC Ensembl
Outerchr3:37772503..37817755hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3845253
hg1945253
hg1845253
hg1745253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5955
SamplesNA19129
Known GenesITGA9
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)nsv3765
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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