A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878673



Internal ID22653639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58581945..58586486hg38UCSC Ensembl
chr19:59093312..59097853hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg384542
hg194542
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479370
Samples
Known GenesCENPBD1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878673
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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