A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3511



Internal ID15201442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:37123197..37138654hg38UCSC Ensembl
Outerchr21:38495497..38510954hg19UCSC Ensembl
Outerchr21:37417367..37432824hg18UCSC Ensembl
Outerchr21:37417367..37432824hg17UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg385357
hg195357
hg185357
hg175357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7722
SamplesNA12156
Known GenesTTC3
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)nsv3511
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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