A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553651



Internal ID20926762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61194952..61196096hg38UCSC Ensembl
chr2:61422087..61423231hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg381145
hg191145
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257699
Samples
Known GenesUSP34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553651
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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