A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18001472



Internal ID20568512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53755298..53762289hg38UCSC Ensembl
chr12:54149082..54156073hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg386992
hg196992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459871
Supporting Variants
Samples
Known GenesCISTR-ACT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18001472
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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