A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849121



Internal ID22624056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119576295..119578122hg38UCSC Ensembl
chr8:120588535..120590362hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg381828
hg191828
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505705
Samples
Known GenesENPP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849121
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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