A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511786



Internal ID22569738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135784073..135785249hg38UCSC Ensembl
chr9:138675919..138677095hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381177
hg191177
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849877
Supporting Variants
Samples
Known GenesKCNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511786
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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