A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4149



Internal ID15548829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:185945853..185977747hg38UCSC Ensembl
Outerchr3:185663641..185695536hg19UCSC Ensembl
Outerchr3:187146335..187178230hg18UCSC Ensembl
Outerchr3:187146343..187178238hg17UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg387606
hg197606
hg187606
hg177606
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10382
SamplesNA18956
Known GenesLOC344887
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)nsv4149
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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