A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869578



Internal ID22644513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14548096..14555200hg38UCSC Ensembl
chr19:14658908..14666012hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg387105
hg197105
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473229
Samples
Known GenesTECR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869578
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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