A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834172



Internal ID22609107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99901845..99908325hg38UCSC Ensembl
chr2:100518307..100524787hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg386481
hg196481
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483089
Samples
Known GenesAFF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834172
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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