A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424896



Internal ID203869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32203042..32203366hg38UCSC Ensembl
chr1:32668643..32668967hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903598
Samples
Known GenesCCDC28B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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