A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357731



Internal ID21015284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151325925..151326518hg38UCSC Ensembl
chr3:151043713..151044306hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096606
Samples
Known GenesMED12L, P2RY13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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