A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021285



Internal ID21930628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29508299..29508350hg38UCSC Ensembl
chr12:29661232..29661283hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600484
Samples
Known GenesTMTC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021285
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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