A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049596



Internal ID20616636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100571701..100574100hg38UCSC Ensembl
chr1:101037257..101039656hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00432


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