A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047657



Internal ID19136876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:96363477..96423730hg38UCSC Ensembl
Innerchr10:98123234..98183487hg19UCSC Ensembl
Innerchr10:98113224..98173477hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3860254
hg1960254
hg1860254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518839
Samples
Known GenesTLL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047657
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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