A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325338



Internal ID20858469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226162360..226164130hg38UCSC Ensembl
chr1:226350061..226351831hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg381771
hg191771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058401
Samples
Known GenesACBD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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