A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533007



Internal ID20906368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25312530..25312840hg38UCSC Ensembl
chr18:22892494..22892804hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039534
Samples
Known GenesZNF521
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533007
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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