A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014929



Internal ID21924272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123254333..123254468hg38UCSC Ensembl
chr10:125013849..125013984hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584195
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014929
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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