A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589351



Internal ID20962422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53536391..53536741hg38UCSC Ensembl
chr12:53930175..53930525hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231339
Samples
Known GenesATF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589351
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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