A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322875



Internal ID20855990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110409549..110413036hg38UCSC Ensembl
chr1:110952171..110955658hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg383488
hg193488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050851
Samples
Known GenesLAMTOR5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322875
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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