A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873481



Internal ID22648428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153419111..153428488hg38UCSC Ensembl
chr1:153391587..153400964hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg389378
hg199378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360142
Samples
Known GenesS100A7A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873481
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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