A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551690



Internal ID20924822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:217635979..217636695hg38UCSC Ensembl
chr1:217809321..217810037hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248620
Samples
Known GenesSPATA17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551690
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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