A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384235



Internal ID21041788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46635867..46647628hg38UCSC Ensembl
chr4:46637884..46649645hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3811762
hg1911762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384235
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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