A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833595



Internal ID22608530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4997260..4999559hg38UCSC Ensembl
chr2:5137393..5139692hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486213
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833595
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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