A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519579



Internal ID18471174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124738468..124800091hg38UCSC Ensembl
Innerchr10:126427037..126488660hg19UCSC Ensembl
Innerchr10:126417027..126478650hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3861624
hg1961624
hg1861624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051396
Supporting Variants
Samples
Known GenesFAM53B, METTL10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519579
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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