A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18114399



Internal ID20681439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163678985..163734578hg38UCSC Ensembl
chr4:164600137..164655730hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3855594
hg1955594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385627
Supporting Variants
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18114399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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