A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169980



Internal ID21314041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:60798853..60805386hg38UCSC Ensembl
Outerchr10:60794742..60811063hg38UCSC Ensembl
Innerchr10:62558611..62565144hg19UCSC Ensembl
Outerchr10:62554500..62570821hg19UCSC Ensembl
Innerchr10:62228617..62235150hg18UCSC Ensembl
Outerchr10:62224506..62240827hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3816322
hg1916322
hg1816322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252252, nssv14250641
SamplesSNI_6, SNI_15
Known GenesCDK1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169980
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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