A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485871



Internal ID22543784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1239628..1280651hg38UCSC Ensembl
chr2:1243400..1284423hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3841024
hg1941024
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831202
Supporting Variants
Samples
Known GenesSNTG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485871
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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