A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430031



Internal ID22487901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30677201..30677576hg38UCSC Ensembl
chr8:30534718..30535093hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912957
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430031
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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