A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368633



Internal ID21026186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87186577..87519943hg38UCSC Ensembl
chr3:87235727..87569093hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg38333367
hg19333367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104166
Samples
Known GenesCHMP2B, MIR4795, POU1F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368633
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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