A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096566



Internal ID20663606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15032564..15033092hg38UCSC Ensembl
chr3:15074071..15074599hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366178
Supporting Variants
Samples
Known GenesNR2C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00076


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