A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557569



Internal ID20930640
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 StatusM
Merged Variants
Supporting Variantsnssv18265983
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)nsv6557569
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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