A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538185



Internal ID20911508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164673693..164674252hg38UCSC Ensembl
chr2:165530203..165530762hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255819
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538185
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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