A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451794



Internal ID22509666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6171184..6183359hg38UCSC Ensembl
chr10:6213147..6225322hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3812176
hg1912176
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847588
Supporting Variants
Samples
Known GenesPFKFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451794
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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