A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554907



Internal ID20927997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:217636132..217636196hg38UCSC Ensembl
chr1:217809474..217809538hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248621
Samples
Known GenesSPATA17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554907
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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