A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360171



Internal ID21017724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141527100..141527733hg38UCSC Ensembl
chr3:141245942..141246575hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094307
Samples
Known GenesRASA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360171
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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