A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104702



Internal ID22013935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10685912..10687066hg38UCSC Ensembl
chr2:10826038..10827192hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534897
Samples
Known GenesNOL10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104702
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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