A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850214



Internal ID22625149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99548352..99555607hg38UCSC Ensembl
chr14:100014689..100021944hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg387256
hg197256
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470247
Samples
Known GenesCCDC85C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850214
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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