A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365363



Internal ID22591032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173505762..173505943hg38UCSC Ensembl
chr1:173474901..173475082hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870846
Supporting Variants
Samples
Known GenesSLC9C2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365363
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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