A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344748



Internal ID21002301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145025452..145025775hg38UCSC Ensembl
chr2:145783019..145783342hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078194
Samples
Known GenesTEX41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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