A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963726



Internal ID22738661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36322497..36326940hg38UCSC Ensembl
chr21:37694795..37699238hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg384444
hg194444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397876
Samples
Known GenesMORC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963726
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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