A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531888



Internal ID20905249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45140301..45141600hg38UCSC Ensembl
chr18:42720266..42721565hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041214
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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