A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581505



Internal ID20954576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60452638..60453482hg38UCSC Ensembl
chr17:58529999..58530843hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38845
hg19845
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243079
Samples
Known GenesAPPBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581505
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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