A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382432



Internal ID21039985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87650901..87652800hg38UCSC Ensembl
chr4:88572053..88573952hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121788
Samples
Known GenesDMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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