A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129596



Internal ID21465213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22607378..22607440hg38UCSC Ensembl
chr4:22609001..22609063hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574943
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129596
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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