A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354695



Internal ID22580364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6766515..6766725hg38UCSC Ensembl
chr12:6875681..6875891hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920136
Supporting Variants
Samples
Known GenesPTMS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354695
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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