A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384343



Internal ID22442213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32865248..32865381hg38UCSC Ensembl
chr1:33330849..33330982hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869931
Supporting Variants
Samples
Known GenesFNDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384343
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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