A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887438



Internal ID22662430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241801567..241826909hg38UCSC Ensembl
chr1:241964869..241990211hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3825343
hg1925343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352671
Samples
Known GenesWDR64
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887438
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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