A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584042



Internal ID20957113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92671805..92672518hg38UCSC Ensembl
chr12:93065581..93066294hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1650n223
Supporting Variantsnssv18229067
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584042
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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