A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468620



Internal ID22526509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158292101..158301504hg38UCSC Ensembl
chr1:158261891..158271294hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg389404
hg199404
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828168
Supporting Variants
Samples
Known GenesCD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468620
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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