A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087907



Internal ID20654947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5158401..5159700hg38UCSC Ensembl
chr2:5298534..5299833hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346948
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00225


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