A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357221



Internal ID21014774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:118932425..118979466hg38UCSC Ensembl
chr3:118651272..118698313hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg3847042
hg1947042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094526
Samples
Known GenesIGSF11, IGSF11-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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