A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467291



Internal ID21124844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43720549..43727768hg38UCSC Ensembl
chr11:43742099..43749318hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg387220
hg197220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991370
Samples
Known GenesHSD17B12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467291
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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