A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493369



Internal ID21150922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124151737..124152257hg38UCSC Ensembl
chr12:124636283..124636803hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997256
Samples
Known GenesZNF664-FAM101A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493369
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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