A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3884



Internal ID15548538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:76597726..76631513hg38UCSC Ensembl
Outerchr3:76646877..76680664hg19UCSC Ensembl
Outerchr3:76729567..76763354hg18UCSC Ensembl
Outerchr3:76729567..76763354hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg387212
hg197212
hg187212
hg177212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv310
SamplesNA19240
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)nsv3884
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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