A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370473



Internal ID21028026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185772390..185773943hg38UCSC Ensembl
chr3:185490178..185491731hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg381554
hg191554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098253
Samples
Known GenesIGF2BP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370473
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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