A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560101



Internal ID333115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4086049..4091264hg38UCSC Ensembl
chr10:4128241..4133456hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385216
hg195216
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560101
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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