A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5550829



Internal ID324337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12916023..12916031hg38UCSC Ensembl
chr10:12958023..12958031hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030213
Samples
Known GenesCCDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5550829
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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