A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263839



Internal ID20830879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151269541..154434055hg38UCSC Ensembl
chr4:152190693..155355207hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383164515
hg193164515
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572617
Supporting Variants
Samples
Known GenesANXA2P1, ARFIP1, DCHS2, DEAR, DKFZP434I0714, FAM160A1, FBXW7, FHDC1, KIAA0922, MIR3140, MIR4453, MND1, PET112, PRSS48, RNF175, SFRP2, TIGD4, TLR2, TMEM154, TRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263839
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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