A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212798



Internal ID20779838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177644827..177888320hg38UCSC Ensembl
chr4:178565981..178809474hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38243494
hg19243494
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391945
Supporting Variants
Samples
Known GenesLINC01098, LINC01099
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212798
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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