A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603661



Internal ID21552326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1612551..1612906hg38UCSC Ensembl
chr19:1612550..1612905hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103224
SamplesHG00731
Known GenesTCF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603661
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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