A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18082660



Internal ID20649700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2084201..2130200hg38UCSC Ensembl
chr2:2087973..2133972hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3846000
hg1946000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344144
Supporting Variants
Samples
Known GenesMYT1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18082660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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