A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749251



Internal ID20525281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15915717..15921770hg38UCSC Ensembl
chr10:15957716..15963769hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386054
hg196054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275113
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749251
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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