A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331852



Internal ID20865019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226173801..226193300hg38UCSC Ensembl
chr1:226361502..226381001hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3819500
hg1919500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058402
Samples
Known GenesACBD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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