A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954166



Internal ID21374237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14912807..14912981hg38UCSC Ensembl
chr10:14954806..14954980hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181456
SamplesHG002
Known GenesDCLRE1C
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954166
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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