A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3557617



Internal ID22426423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5810256..5810556hg38UCSC Ensembl
chr5:5810369..5810669hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14319399, nssv14319398, nssv14319401, nssv14319400
SamplesNA19238, HG00731, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3557617
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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