A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14305663



Internal ID22323614
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3557387
Supporting Variants
SamplesNA19240
Known GenesTRAF3IP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14305663
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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