A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18114459



Internal ID20681499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164131451..164131885hg38UCSC Ensembl
chr4:165052603..165053037hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375641
Supporting Variants
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18114459
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00076


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