A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3558313



Internal ID22427116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97445822..97460380hg38UCSC Ensembl
chr7:97075134..97089692hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3814559
hg1914559
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335525, nssv14335523, nssv14335524
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3558313
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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