A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149353



Internal ID21423030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35089865..35089938hg38UCSC Ensembl
chr8:34947383..34947456hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569813
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149353
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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