A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575583



Internal ID21524012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:237883963..237884016hg38UCSC Ensembl
chr1:238047263..238047316hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063351
SamplesNA19238
Known GenesLOC100130331, ZP4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575583
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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