A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531899



Internal ID20905260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58585441..58588740hg38UCSC Ensembl
chr18:56252673..56255972hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042338
Samples
Known GenesALPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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