A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260938



Internal ID20827978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86913968..87825588hg38UCSC Ensembl
chr2:87141091..88125107hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38911621
hg19984017
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547455
Supporting Variants
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)nssv18260938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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