A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571422



Internal ID20944493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146996555..151115323hg38UCSC Ensembl
chr6:147317691..151436459hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg384118769
hg194118769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273206
Samples
Known GenesGINM1, IYD, KATNA1, LATS1, LOC100128176, LRP11, MTHFD1L, NUP43, PCMT1, PLEKHG1, PPIL4, PPP1R14C, RAET1E, RAET1E-AS1, RAET1G, RAET1K, RAET1L, RPS18P9, SAMD5, SASH1, STXBP5, STXBP5-AS1, SUMO4, TAB2, ULBP1, ULBP2, ULBP3, UST, ZC3H12D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571422
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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