A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545694



Internal ID20918919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:187776500..187777167hg38UCSC Ensembl
chr2:188641227..188641894hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545694
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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