A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367875



Internal ID21025428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188604736..188605304hg38UCSC Ensembl
chr3:188322524..188323092hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100266
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367875
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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