A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482971



Internal ID22540877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9687100..9688499hg38UCSC Ensembl
chr2:9827229..9828628hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834214
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482971
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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