A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531268



Internal ID20904629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49077866..49088311hg38UCSC Ensembl
chr18:46604236..46614681hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3810446
hg1910446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042113
Samples
Known GenesDYM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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