A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463530



Internal ID21121083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76992898..76995268hg38UCSC Ensembl
chr11:76703942..76706312hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg382371
hg192371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994351
Samples
Known GenesACER3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463530
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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