A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211923



Internal ID20778963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53903017..53948698hg38UCSC Ensembl
chr4:54769184..54814865hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3845682
hg1945682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387736
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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