A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828398



Internal ID22603333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168242487..168245286hg38UCSC Ensembl
chr1:168211725..168214524hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456156
Samples
Known GenesSFT2D2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828398
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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