A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065637



Internal ID20632677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94554434..94554734hg38UCSC Ensembl
chr1:95019990..95020290hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327189
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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