A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341194



Internal ID20998747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25860298..25863238hg38UCSC Ensembl
chr2:26083167..26086107hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg382941
hg192941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085629
Samples
Known GenesASXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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