A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488193



Internal ID22546110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:154962227..154973689hg38UCSC Ensembl
chr2:155818739..155830201hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3811463
hg1911463
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488193
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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