A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853497



Internal ID22628432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96468535..96470362hg38UCSC Ensembl
chr14:96934872..96936699hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381828
hg191828
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470396
Samples
Known GenesAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853497
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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