A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581587



Internal ID20954658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32086756..32088604hg38UCSC Ensembl
chr12:32239690..32241538hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg381849
hg191849
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581587
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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