A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489049



Internal ID266340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15367145..15487291hg38UCSC Ensembl
chr10:15409144..15529290hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38120147
hg19120147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032073
Samples
Known GenesFAM171A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489049
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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