A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143585



Internal ID342786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87284368..87454368hg38UCSC Ensembl
chr10:89044125..89214125hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38170001
hg19170001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036811
Samples
Known GenesLINC00864, LOC439994, NUTM2A-AS1, NUTM2D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143585
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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