A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582944



Internal ID20956015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48146214..48146924hg38UCSC Ensembl
chr17:46223576..46224286hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242504
Samples
Known GenesSKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582944
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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