A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574395



Internal ID20947466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87923661..89968732hg38UCSC Ensembl
chr4:88844813..90889883hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg382045072
hg192045071
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5354n223
Supporting Variantsnssv18266732
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)nsv6574395
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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