A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063442



Internal ID21486629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223888108..223888831hg38UCSC Ensembl
chr1:224075810..224076533hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567535
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063442
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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