A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384283



Internal ID21041836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121639846..121654342hg38UCSC Ensembl
chr4:122561001..122575497hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3814497
hg1914497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108998
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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