A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18076659



Internal ID20643699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105932326..105941028hg38UCSC Ensembl
chr2:106548782..106557484hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg388703
hg198703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351993
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18076659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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