A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3924



Internal ID15548582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:101169817..101190219hg38UCSC Ensembl
Outerchr3:100888661..100909063hg19UCSC Ensembl
Outerchr3:102371351..102391753hg18UCSC Ensembl
Outerchr3:102371351..102391753hg17UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg385498
hg195498
hg185498
hg175498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3105
SamplesNA18555
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)nsv3924
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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