A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872730



Internal ID22647671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58545740..58554893hg38UCSC Ensembl
chr19:59057107..59066260hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg389154
hg199154
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1098n209
Supporting Variantsnssv17479359
Samples
Known GenesCHMP2A, MIR6807, TRIM28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872730
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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