A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105446



Internal ID21477826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47070058..47070988hg38UCSC Ensembl
chr19:47573315..47574245hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589543
Supporting Variants
SamplesHG03486
Known GenesZC3H4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105446
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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