A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555696



Internal ID328847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23443760..23443881hg38UCSC Ensembl
chr7:23483379..23483500hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994508
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555696
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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