A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202505



Internal ID22351661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64695200..64696559hg38UCSC Ensembl
chr3:64680876..64682235hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381360
hg191360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14306683
SamplesHG00731
Known GenesADAMTS9-AS2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202505
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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