A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380835



Internal ID21038388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55068101..55071600hg38UCSC Ensembl
chr4:55934268..55937767hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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