A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571892



Internal ID20944963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60444375..60448807hg38UCSC Ensembl
chr8:61356934..61361366hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg384433
hg194433
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7362n223
Supporting Variantsnssv18278376
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571892
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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