A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557693



Internal ID330782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11817726..11825678hg38UCSC Ensembl
chr18:11817725..11825677hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg387953
hg197953
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716238
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557693
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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