A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381074



Internal ID22438944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32499998..32504762hg38UCSC Ensembl
chr1:32965599..32970363hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg384765
hg194765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381074
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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