A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358501



Internal ID22584170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103984961..103986901hg38UCSC Ensembl
chr12:104378739..104380679hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381941
hg191941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928840
Supporting Variants
Samples
Known GenesTDG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358501
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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