A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870672



Internal ID22645608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37234655..37236054hg38UCSC Ensembl
chr19:37725557..37726956hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475337
Samples
Known GenesZNF383
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870672
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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