A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373622



Internal ID21031175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7087046..7091720hg38UCSC Ensembl
chr4:7088773..7093447hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg384675
hg194675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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