A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169820



Internal ID21313631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129014291..129017735hg38UCSC Ensembl
Outerchr10:129013386..129030109hg38UCSC Ensembl
Innerchr10:130812555..130815999hg19UCSC Ensembl
Outerchr10:130811650..130828373hg19UCSC Ensembl
Innerchr10:130702545..130705989hg18UCSC Ensembl
Outerchr10:130701640..130718363hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3816724
hg1916724
hg1816724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246876
SamplesSNI_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169820
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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