A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591737



Internal ID20964808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95617507..95617877hg38UCSC Ensembl
chr12:96011283..96011653hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591737
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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