A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280169



Internal ID20847209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137713210..137713855hg38UCSC Ensembl
chr9:140607662..140608307hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559630
Supporting Variants
Samples
Known GenesEHMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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