A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14241569



Internal ID21312986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125412506..125421496hg38UCSC Ensembl
Outerchr10:125408170..125425349hg38UCSC Ensembl
Innerchr10:127101075..127110065hg19UCSC Ensembl
Outerchr10:127096739..127113918hg19UCSC Ensembl
Innerchr10:127091065..127100055hg18UCSC Ensembl
Outerchr10:127086729..127103908hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3817180
hg1917180
hg1817180
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169884
Supporting Variants
SamplesSNI_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14241569
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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