A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505935



Internal ID22563880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30077097..30080646hg38UCSC Ensembl
chr8:29934613..29938162hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383550
hg193550
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854550
Supporting Variants
Samples
Known GenesMIR548O2, TMEM66
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505935
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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