A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831079



Internal ID22606014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10764838..10770087hg38UCSC Ensembl
chr2:10904964..10910213hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385250
hg195250
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484946
Samples
Known GenesATP6V1C2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831079
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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