A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473652



Internal ID21131205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65095103..65102911hg38UCSC Ensembl
chr12:65488883..65496691hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg387809
hg197809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002963
Samples
Known GenesWIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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