A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468923



Internal ID21126476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119631123..119655149hg38UCSC Ensembl
chr11:119501834..119525859hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3824027
hg1924026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987237
Samples
Known GenesPVRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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