A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873605



Internal ID22648553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36058274..36059273hg38UCSC Ensembl
chr21:37430572..37431571hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480335, nssv17480334
Samples
Known GenesSETD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873605
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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