A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211924



Internal ID20778964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53936501..53937500hg38UCSC Ensembl
chr4:54802668..54803667hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211924
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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