A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321867



Internal ID20854975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111133601..111136100hg38UCSC Ensembl
chr1:111676223..111678722hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050892
Samples
Known GenesDRAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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