A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475275



Internal ID21132828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66250101..66254900hg38UCSC Ensembl
chr11:66017572..66022371hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992560
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475275
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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