A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460239



Internal ID21117792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53509650..53510102hg38UCSC Ensembl
chr12:53903434..53903886hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001462
Samples
Known GenesATF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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