A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487949



Internal ID265270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35887315..35889222hg38UCSC Ensembl
chr10:36176243..36178150hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381908
hg191908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487949
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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