A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506815



Internal ID22564763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127741266..127748470hg38UCSC Ensembl
chr8:128753512..128760716hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg387205
hg197205
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850629
Supporting Variants
Samples
Known GenesMYC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506815
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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