A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3972



Internal ID15201949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:122030645..122062809hg38UCSC Ensembl
Outerchr3:121749492..121781656hg19UCSC Ensembl
Outerchr3:123232182..123264346hg18UCSC Ensembl
Outerchr3:123232182..123264346hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg387270
hg197270
hg187270
hg177270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7027
SamplesNA12156
Known GenesCD86
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)nsv3972
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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