A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386372



Internal ID21043925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120012772..120042663hg38UCSC Ensembl
chr4:120933927..120963818hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3829892
hg1929892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107815
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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