A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3933244



Internal ID21353313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18741447..18741597hg38UCSC Ensembl
chr10:19030376..19030526hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15180934
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3933244
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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