A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863788



Internal ID22638723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98199717..98216759hg38UCSC Ensembl
chr7:97829029..97846071hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3817043
hg1917043
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504269
Samples
Known GenesBHLHA15, LMTK2, TECPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863788
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer