A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038896



Internal ID21948239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110839127..110839221hg38UCSC Ensembl
chr13:111491474..111491568hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038896
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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