A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555924



Internal ID20928995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110996923..110997657hg38UCSC Ensembl
chr6:111318126..111318860hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268470
Samples
Known GenesRPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555924
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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