A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037070



Internal ID21946413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50981916..50981975hg38UCSC Ensembl
chr18:48508286..48508345hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637051
Samples
Known GenesELAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037070
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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