A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556635



Internal ID20929706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110880811..110881703hg38UCSC Ensembl
chr6:111202014..111202906hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38893
hg19893
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6366n223
Supporting Variantsnssv18268451
Samples
Known GenesAMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556635
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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