A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522877



Internal ID20896238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58014535..58022274hg38UCSC Ensembl
chr18:55681767..55689506hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg387740
hg197740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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