A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553936



Internal ID20927046
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 Variantsdgv3955n223
Supporting Variantsnssv18260937
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)nsv6553936
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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