A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570589



Internal ID20943660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39837502..39838759hg38UCSC Ensembl
chr8:39695021..39696278hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg381258
hg191258
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7319n223
Supporting Variantsnssv18277971
Samples
Known GenesADAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570589
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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