A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18112633



Internal ID20679673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20000320..20006833hg38UCSC Ensembl
chr4:20001943..20008456hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg386514
hg196514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370299
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18112633
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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