A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592657



Internal ID20965728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:91157910..91158827hg38UCSC Ensembl
chr12:91551687..91552604hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1648n223
Supporting Variantsnssv18223088
Samples
Known GenesDCN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592657
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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