A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265983



Internal ID20833023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70947674..74191820hg38UCSC Ensembl
chr4:71813391..75057537hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg383244147
hg193244147
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557569
Supporting Variants
Samples
Known GenesADAMTS3, AFM, AFP, ALB, ANKRD17, COX18, CXCL1, CXCL2, CXCL3, CXCL5, CXCL6, DCK, GC, IL8, LOC728040, MOB1B, MTHFD2L, NPFFR2, PF4, PF4V1, PPBP, PPBPP2, RASSF6, SLC4A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265983
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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