A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382280



Internal ID21039833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40224043..40224578hg38UCSC Ensembl
chr4:40225663..40226198hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117093
Samples
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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