A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462952



Internal ID21120505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62876849..62879351hg38UCSC Ensembl
chr11:62644321..62646823hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382503
hg192503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993240
Samples
Known GenesSLC3A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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