A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3853



Internal ID15548504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:64952507..64986465hg38UCSC Ensembl
Outerchr3:64938182..64972140hg19UCSC Ensembl
Outerchr3:64913222..64947180hg18UCSC Ensembl
Outerchr3:64913222..64947180hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg385467
hg195467
hg185467
hg175467
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7819
SamplesNA12156
Known GenesADAMTS9-AS2, MIR548A2, MIR548AN
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)nsv3853
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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