A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392601



Internal ID22450471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:170155382..170155445hg38UCSC Ensembl
chr2:171011892..171011955hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892543
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392601
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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