A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3445



Internal ID15201369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63153644..63174462hg38UCSC Ensembl
Outerchr20:61784996..61805814hg19UCSC Ensembl
Outerchr20:61255441..61276259hg18UCSC Ensembl
Outerchr20:61255441..61276259hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385540
hg195540
hg185540
hg175540
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1614, nssv4548, nssv3068
SamplesNA12878, NA18555, NA19240
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)nsv3445
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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