A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18078761



Internal ID20645801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14781933..14789415hg38UCSC Ensembl
chr2:14922057..14929539hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg387483
hg197483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6338868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18078761
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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