A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565036



Internal ID20938107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38545481..38546844hg38UCSC Ensembl
chr6:38513257..38514620hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270789
Samples
Known GenesBTBD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565036
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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