A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749230



Internal ID20525260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122633351..122633416hg38UCSC Ensembl
chr10:124392867..124392932hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295232
Samples
Known GenesDMBT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749230
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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