A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248700



Internal ID20815740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173825570..173826070hg38UCSC Ensembl
chr1:173794708..173795208hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545689
Supporting Variants
Samples
Known GenesDARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248700
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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