A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342502



Internal ID21000055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157728901..157730000hg38UCSC Ensembl
chr2:158585413..158586512hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342502
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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