A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921929



Internal ID22697153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63664771..63672742hg38UCSC Ensembl
chr10:65424531..65432502hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg387972
hg197972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17349728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921929
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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