A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603919



Internal ID21795966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7199827..7199928hg38UCSC Ensembl
chr12:7352423..7352524hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025193
Supporting Variants
Samples
Known GenesPEX5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603919
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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