A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3325



Internal ID15547923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:21085506..21119164hg38UCSC Ensembl
Outerchr20:21066147..21099805hg19UCSC Ensembl
Outerchr20:21014147..21047805hg18UCSC Ensembl
Outerchr20:21014147..21047805hg17UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg385772
hg195772
hg185772
hg175772
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7662
SamplesNA12156
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)nsv3325
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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