A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616104



Internal ID21808151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29662662..29664174hg38UCSC Ensembl
chr12:29815595..29817107hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg381513
hg191513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036112
Supporting Variants
Samples
Known GenesTMTC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616104
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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