A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5903



Internal ID15196792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:36007961..36040889hg38UCSC Ensembl
Outerchr21:37380259..37413187hg19UCSC Ensembl
Outerchr21:36302129..36335057hg18UCSC Ensembl
Outerchr21:36302129..36335057hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg386360
hg196360
hg186360
hg176360
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3504
Supporting Variants
SamplesNA19129
Known GenesSETD4
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)nssv5903
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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