A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485809



Internal ID22543722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119009361..119041568hg38UCSC Ensembl
chr2:119766937..119799144hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3832208
hg1932208
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831191
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485809
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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