A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554911



Internal ID20928001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10743996..10744684hg38UCSC Ensembl
chr2:10884122..10884810hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256443
Samples
Known GenesATP6V1C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554911
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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