A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531976



Internal ID20905337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74439545..74439965hg38UCSC Ensembl
chr18:72106780..72107200hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043911
Samples
Known GenesFAM69C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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