A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362496



Internal ID21020049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151402633..151403009hg38UCSC Ensembl
chr3:151120421..151120797hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096612
Samples
Known GenesMED12L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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