A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450932



Internal ID22508805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76711783..76717282hg38UCSC Ensembl
chr12:77105563..77111062hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848171
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450932
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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