A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106879



Internal ID21456301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7745632..7745769hg38UCSC Ensembl
chr19:7810518..7810655hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590407
Supporting Variants
SamplesHG02492
Known GenesCD209
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106879
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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