A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938858



Internal ID21358927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70918724..70918879hg38UCSC Ensembl
chr10:72678481..72678636hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181523
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938858
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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