A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403737



Internal ID22461607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203355764..203360654hg38UCSC Ensembl
chr2:204220487..204225377hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg384891
hg194891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906479
Supporting Variants
Samples
Known GenesABI2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403737
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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