A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489290



Internal ID22547209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207173031..207177161hg38UCSC Ensembl
chr2:208037755..208041885hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg384131
hg194131
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832435
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489290
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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