A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535994



Internal ID20909348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104670638..104670790hg38UCSC Ensembl
chr2:105287096..105287248hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535994
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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