A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929752



Internal ID21349822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179638153..179638920hg38UCSC Ensembl
chr1:179607288..179608055hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15178488
SamplesHG002
Known GenesTDRD5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929752
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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