A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572318



Internal ID21520706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187304411..187304716hg38UCSC Ensembl
chr4:188225565..188225870hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128926
SamplesHG00732
Known GenesLOC339975
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572318
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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