A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364576



Internal ID22590245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24683169..24683468hg38UCSC Ensembl
chr1:25009660..25009959hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869203
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364576
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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