A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007999



Internal ID21917342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112455202..112455257hg38UCSC Ensembl
chr10:114214961..114215016hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586094
Samples
Known GenesVTI1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007999
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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