A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098749



Internal ID20665789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:175191500..175192600hg38UCSC Ensembl
chr3:174909290..174910390hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371703
Supporting Variants
Samples
Known GenesNAALADL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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