A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535986



Internal ID20909340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202366363..202367569hg38UCSC Ensembl
chr2:203231086..203232292hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381207
hg191207
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535986
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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