A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953494



Internal ID21373563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45726859..45727184hg38UCSC Ensembl
chr3:45768351..45768676hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15178971
SamplesHG002
Known GenesSACM1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953494
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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