A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104710



Internal ID21493812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3938290..3938380hg38UCSC Ensembl
chr19:3938288..3938378hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604026
Supporting Variants
SamplesNA19238
Known GenesNMRK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104710
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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