A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14243435



Internal ID21310724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125407461..125421496hg38UCSC Ensembl
Outerchr10:125404278..125425349hg38UCSC Ensembl
Innerchr10:127096030..127110065hg19UCSC Ensembl
Outerchr10:127092847..127113918hg19UCSC Ensembl
Innerchr10:127086020..127100055hg18UCSC Ensembl
Outerchr10:127082837..127103908hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3821072
hg1921072
hg1821072
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169884
Supporting Variants
SamplesPML_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14243435
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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