A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556507



Internal ID20929578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182870691..182871820hg38UCSC Ensembl
chr3:182588479..182589608hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381130
hg191130
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5115n223
Supporting Variantsnssv18261832
Samples
Known GenesATP11B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556507
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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