A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582595



Internal ID20955666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76173619..76174278hg38UCSC Ensembl
chr12:76567399..76568058hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582595
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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