A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032033



Internal ID89060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14950103..15005437hg38UCSC Ensembl
chr10:14992102..15047436hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3855335
hg1955335
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483255
Supporting Variants
Samples
Known GenesDCLRE1C, MEIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032033
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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