A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585436



Internal ID20958507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52938000..52938204hg38UCSC Ensembl
chr12:53331784..53331988hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226938
Samples
Known GenesKRT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585436
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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