A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18075603



Internal ID20642643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113686967..113688105hg38UCSC Ensembl
chr2:114444544..114445682hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381139
hg191139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351153
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18075603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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