A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354848



Internal ID21012401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135818769..135819655hg38UCSC Ensembl
chr2:136576339..136577225hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38887
hg19887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077911
Samples
Known GenesLCT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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