A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869263



Internal ID22644198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7704304..7712025hg38UCSC Ensembl
chr19:7769190..7776911hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387722
hg197722
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869263
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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