A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549450



Internal ID20922611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:155324258..155419329hg38UCSC Ensembl
chr2:156180770..156275841hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3895072
hg1995072
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254663
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549450
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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