A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531138



Internal ID20904499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:78303174..78308682hg38UCSC Ensembl
chr18:76063174..76068682hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg385509
hg195509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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