A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870144



Internal ID22645079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36916406..36927650hg38UCSC Ensembl
chr19:37407308..37418552hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3811245
hg1911245
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475315
Samples
Known GenesZNF568
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870144
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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