A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391245



Internal ID21048798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:179400405..179431081hg38UCSC Ensembl
chr4:180321559..180352235hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3830677
hg1930677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391245
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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