A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226532



Internal ID22369301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7207479..7207530hg38UCSC Ensembl
chr10:7249441..7249492hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327281, nssv14410691, nssv14327285, nssv14327283, nssv14327282, nssv14327280, nssv14327286, nssv14327284, nssv14327279, nssv14436295, nssv14466376
SamplesHG00512, NA19238, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesSFMBT2
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226532
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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