A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366181



Internal ID21023734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48018963..48041957hg38UCSC Ensembl
chr3:48060453..48083447hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3822995
hg1922995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100794
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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