A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380069



Internal ID21037622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101230281..101241219hg38UCSC Ensembl
chr4:102151438..102162376hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3810939
hg1910939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106125
Samples
Known GenesMIR8066, PPP3CA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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