A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480683



Internal ID22538587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173920857..173933037hg38UCSC Ensembl
chr2:174785585..174797765hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3812181
hg1912181
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831440
Supporting Variants
Samples
Known GenesSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480683
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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