A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535844



Internal ID20909198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61118399..61119854hg38UCSC Ensembl
chr2:61345534..61346989hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg381456
hg191456
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257695
Samples
Known GenesKIAA1841
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535844
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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