A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370753



Internal ID21028306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154336268..154336896hg38UCSC Ensembl
chr3:154054057..154054685hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370753
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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