A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593551



Internal ID20966622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64934251..64935225hg38UCSC Ensembl
chr15:65226451..65227424hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38975
hg19974
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238863
Samples
Known GenesANKDD1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593551
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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