A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436634



Internal ID21094187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18242330..18246014hg38UCSC Ensembl
chr11:18263877..18267561hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg383685
hg193685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988641
Samples
Known GenesSAA2, SAA2-SAA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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