A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936935



Internal ID21357004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4815475..4815695hg38UCSC Ensembl
chr10:4857667..4857887hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180260
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936935
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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