A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233201



Internal ID20800241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73072985..73073443hg38UCSC Ensembl
chr10:74832743..74833201hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582263
Supporting Variants
Samples
Known GenesP4HA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233201
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00044


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