A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148557



Internal ID21422738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60945305..60957181hg38UCSC Ensembl
chr8:61857864..61869740hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg3811877
hg1911877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580061
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148557
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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