A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085537



Internal ID20652577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24464278..24471240hg38UCSC Ensembl
chr2:24687147..24694109hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg386963
hg196963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352707
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085537
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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