A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371143



Internal ID21028696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151312516..151314759hg38UCSC Ensembl
chr3:151030304..151032547hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382244
hg192244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096605
Samples
Known GenesGPR87, MED12L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371143
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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