A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525914



Internal ID22395292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119063189..119063245hg38UCSC Ensembl
chr5:118398884..118398940hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14322519, nssv14322520, nssv14322518
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525914
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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