A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017961



Internal ID21927304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16295035..16295103hg38UCSC Ensembl
chr10:16337034..16337102hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017961
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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