A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488707



Internal ID22546624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173932439..173936341hg38UCSC Ensembl
chr2:174797167..174801069hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg383903
hg193903
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831441
Supporting Variants
Samples
Known GenesSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488707
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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