A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502409



Internal ID22560349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149668160..149673419hg38UCSC Ensembl
chr6:149989296..149994555hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg385260
hg195260
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844648
Supporting Variants
Samples
Known GenesLATS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502409
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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