A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441182



Internal ID21098735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3055167..3065258hg38UCSC Ensembl
chr11:3076397..3086488hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810092
hg1910092
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182864
Samples
Known GenesCARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441182
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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