A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266731



Internal ID20833771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87923653..89968726hg38UCSC Ensembl
chr4:88844805..90889877hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg382045074
hg192045073
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556594
Supporting Variants
Samples
Known GenesABCG2, FAM13A, FAM13A-AS1, GPRIN3, HERC3, HERC5, HERC6, LOC644248, MMRN1, NAP1L5, PIGY, PKD2, PPM1K, PYURF, SNCA, SPP1, TIGD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266731
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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