A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480090



Internal ID257601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7661353..7661445hg38UCSC Ensembl
chr10:7703316..7703408hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030626
Samples
Known GenesITIH5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480090
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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