A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572043



Internal ID20945114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60276849..60277389hg38UCSC Ensembl
chr8:61189408..61189948hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278371
Samples
Known GenesCA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572043
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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