A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252252



Internal ID21312976
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 Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169980
Supporting Variants
SamplesSNI_6
Known GenesCDK1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252252
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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