A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100667



Internal ID20667707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45678121..45685315hg38UCSC Ensembl
chr3:45719613..45726807hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg387195
hg197195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371510
Supporting Variants
Samples
Known GenesLIMD1, LIMD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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