A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392908



Internal ID21050461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141081077..141083110hg38UCSC Ensembl
chr4:142002231..142004264hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg382034
hg192034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108151
Samples
Known GenesRNF150
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392908
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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