A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084749



Internal ID20651789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:211965703..212059593hg38UCSC Ensembl
chr2:212830428..212924318hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3893891
hg1993891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337773
Supporting Variants
Samples
Known GenesERBB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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