A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355025



Internal ID21012578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144629201..144633300hg38UCSC Ensembl
chr2:145386768..145390867hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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