A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077637



Internal ID20644677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:134986905..134992262hg38UCSC Ensembl
chr2:135744475..135749832hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg385358
hg195358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351740
Supporting Variants
Samples
Known GenesMAP3K19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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