A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182217



Internal ID20749257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34089467..34240956hg38UCSC Ensembl
chr11:34111014..34262503hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38151490
hg19151490
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474754
Supporting Variants
Samples
Known GenesABTB2, CAPRIN1, NAT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182217
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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