A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074650



Internal ID20641690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100011264..100017328hg38UCSC Ensembl
chr2:100627726..100633790hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg386065
hg196065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6348871
Supporting Variants
Samples
Known GenesAFF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074650
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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