A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3876



Internal ID15548529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:73287710..73332724hg38UCSC Ensembl
Outerchr3:73336861..73381875hg19UCSC Ensembl
Outerchr3:73419551..73464565hg18UCSC Ensembl
Outerchr3:73419551..73464565hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3845015
hg1945015
hg1845015
hg1745015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5974
SamplesNA19129
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)nsv3876
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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