A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551134



Internal ID20885700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62311948..62312716hg38UCSC Ensembl
chr2:62539083..62539851hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551134
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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