A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387758



Internal ID21045311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140208808..140225371hg38UCSC Ensembl
chr4:141129962..141146525hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3816564
hg1916564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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