A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569707



Internal ID20942778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16366378..19792903hg38UCSC Ensembl
chr8:16223887..19650414hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383426526
hg193426528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277364
Samples
Known GenesASAH1, CNOT7, CSGALNACT1, FGF20, FGL1, LOC100128993, MICU3, MTMR7, MTUS1, NAT1, NAT2, PCM1, PDGFRL, PSD3, SH2D4A, SLC7A2, VPS37A, ZDHHC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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