A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399991



Internal ID22457861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:228894572..228895190hg38UCSC Ensembl
chr2:229759288..229759906hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901327
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399991
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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