A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359327



Internal ID22584996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111622112..111623674hg38UCSC Ensembl
chr12:112059916..112061478hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg381563
hg191563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928008
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359327
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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