A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443940



Internal ID21101493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3021495..3021991hg38UCSC Ensembl
chr11:3042725..3043221hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180188
Samples
Known GenesCARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443940
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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