A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555669



Internal ID328821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127433595..127436974hg38UCSC Ensembl
chr10:129231859..129235238hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg383380
hg193380
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039087
Samples
Known GenesDOCK1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555669
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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