A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569566



Internal ID20942637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81999954..82000799hg38UCSC Ensembl
chr7:81629270..81630115hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276730
Samples
Known GenesCACNA2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569566
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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