A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361245



Internal ID21018798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148155400..148156910hg38UCSC Ensembl
chr3:147873187..147874697hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381511
hg191511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361245
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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