A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367528



Internal ID21025081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36213245..36213684hg38UCSC Ensembl
chr4:36214867..36215306hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116969
Samples
Known GenesARAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367528
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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