A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349913



Internal ID21007466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23859459..23859591hg38UCSC Ensembl
chr2:24082329..24082461hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084454
Samples
Known GenesATAD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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