A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526690



Internal ID22396073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71317927..71318648hg38UCSC Ensembl
chr3:71367078..71367799hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14305516, nssv14305518, nssv14305517, nssv14305519
SamplesHG00512, NA19238, NA19239, NA19240
Known GenesFOXP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526690
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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