A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482001



Internal ID22539906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203355902..203360676hg38UCSC Ensembl
chr2:204220625..204225399hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg384775
hg194775
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832154
Supporting Variants
Samples
Known GenesABI2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482001
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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