A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462931



Internal ID21120484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124247956..124248657hg38UCSC Ensembl
chr11:124118707..124119408hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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