A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544688



Internal ID20917925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10467813..10468345hg38UCSC Ensembl
chr2:10607939..10608471hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544688
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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