A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526262



Internal ID22395642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172893874..172893938hg38UCSC Ensembl
chr5:172320877..172320941hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7616n152
Supporting Variantsnssv14324509, nssv14324508, nssv14324510
SamplesNA19238, NA19239, NA19240
Known GenesERGIC1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526262
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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