A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383979



Internal ID21041532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:82465986..82471662hg38UCSC Ensembl
chr4:83387139..83392815hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg385677
hg195677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119900
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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