A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437903



Internal ID22495773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30091731..30091976hg38UCSC Ensembl
chr8:29949247..29949492hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910728
Supporting Variants
Samples
Known GenesMIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437903
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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