A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615714



Internal ID21807761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32715770..32715854hg38UCSC Ensembl
chr12:32868704..32868788hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033159
Supporting Variants
Samples
Known GenesDNM1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615714
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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