A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874765



Internal ID22649718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1495451..1533891hg38UCSC Ensembl
chr1:1430831..1469271hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3838441
hg1938441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17349955
Samples
Known GenesATAD3A, ATAD3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874765
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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