A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384675



Internal ID21042228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147301536..147302470hg38UCSC Ensembl
chr4:148222688..148223622hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg38935
hg19935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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