A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587646



Internal ID20960717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56378823..56379592hg38UCSC Ensembl
chr12:56772607..56773376hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233567
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587646
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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