A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869023



Internal ID22643958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51709888..51720871hg38UCSC Ensembl
chr19:52213141..52224124hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3810984
hg1910984
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477954
Samples
Known GenesHAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869023
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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