A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529662



Internal ID22399053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25896164..25896232hg38UCSC Ensembl
chr10:26185093..26185161hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335214, nssv14335212, nssv14335213
SamplesNA19238, HG00731, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529662
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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