A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369618



Internal ID22595287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:199045193..199045503hg38UCSC Ensembl
chr1:199014322..199014632hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874696
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369618
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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