A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464922



Internal ID21122475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57790438..57790918hg38UCSC Ensembl
chr12:58184221..58184701hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001976
Samples
Known GenesTSFM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464922
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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