A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554449



Internal ID327636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14052897..14065327hg38UCSC Ensembl
chr7:14092522..14104952hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3812431
hg1912431
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16993057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554449
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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