A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572666



Internal ID20945737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96987697..97378008hg38UCSC Ensembl
chr6:97435573..97825884hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38390312
hg19390312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272780
Samples
Known GenesKLHL32, MIR548H3, MMS22L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572666
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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