A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936564



Internal ID22711920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68854950..68855831hg38UCSC Ensembl
chr12:69248730..69249611hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38882
hg19882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367892
Samples
Known GenesCPM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936564
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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