A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367892



Internal ID22593561
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 StatusS
Merged Variantsnsv5936564
Supporting Variants
Samples
Known GenesCPM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367892
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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