A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104212



Internal ID21471960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2643314..2643440hg38UCSC Ensembl
chr19:2643312..2643438hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589397
Supporting Variants
SamplesHG03125
Known GenesGNG7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104212
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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