A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521071



Internal ID20894432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49423013..49425981hg38UCSC Ensembl
chr18:46949383..46952351hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg382969
hg192969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042142
Samples
Known GenesDYM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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