A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3955n223



Internal ID22806923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86913704..87825694hg38UCSC Ensembl
chr2:87140827..88125213hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38911991
hg19984387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6547455, nsv6553936
Samples
Known GenesLINC00152, LOC285074, MIR4435-1, MIR4435-2, PLGLB1, PLGLB2, RGPD1, RGPD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3955n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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