A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366979



Internal ID22592648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21412343..21433586hg38UCSC Ensembl
chr12:21565277..21586520hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3821244
hg1921244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366979
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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