A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360635



Internal ID22586304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51178297..51178614hg38UCSC Ensembl
chr12:51572080..51572397hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929404
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360635
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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