A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3232610



Internal ID22372547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101777347..101784976hg38UCSC Ensembl
chr2:102393809..102401438hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg387630
hg197630
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14294091
SamplesNA19238
Known GenesMAP4K4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3232610
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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