A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525120



Internal ID20898481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21671060..21675070hg38UCSC Ensembl
chr18:19251021..19255031hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg384011
hg194011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038965
Samples
Known GenesABHD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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