A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159383



Internal ID21442110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:49534723..49534811hg38UCSC Ensembl
chr7:49574319..49574407hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579812
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159383
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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