A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554547



Internal ID20927640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61105110..61105546hg38UCSC Ensembl
chr2:61332245..61332681hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257691
Samples
Known GenesKIAA1841
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554547
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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