A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3557387



Internal ID22426193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209761990..209762730hg38UCSC Ensembl
chr1:209935335..209936075hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14305662, nssv14305660, nssv14305663, nssv14305489, nssv14305661
SamplesHG00512, NA19238, NA19239, HG00732, NA19240
Known GenesTRAF3IP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3557387
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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