A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263480



Internal ID20830520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108267752..117667773hg38UCSC Ensembl
chr4:109188908..118588928hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg389400022
hg199400021
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572140
Supporting Variants
Samples
Known GenesALPK1, ANK2, AP1AR, ARSJ, C4orf21, C4orf32, CAMK2D, CASP6, CCDC109B, CFI, COL25A1, EGF, ELOVL6, ENPEP, ETNPPL, GAR1, LARP7, LRIT3, MIR1243, MIR1973, MIR302A, MIR302B, MIR302C, MIR302D, MIR367, MIR577, MIR8082, NDST4, NEUROG2, OSTC, PITX2, PLA2G12A, RPL34, RPL34-AS1, RRH, SEC24B, SEC24B-AS1, TIFA, TRAM1L1, UGT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263480
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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