A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449015



Internal ID22506885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29703081..29706544hg38UCSC Ensembl
chr8:29560597..29564060hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383464
hg193464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918347
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449015
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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