A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565715



Internal ID20938786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92114599..92115705hg38UCSC Ensembl
chr9:94876881..94877987hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381107
hg191107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7874n223
Supporting Variantsnssv18281419
Samples
Known GenesSPTLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565715
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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