A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041863



Internal ID18784394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7063546..7188862hg38UCSC Ensembl
Innerchr10:7105508..7230824hg19UCSC Ensembl
Innerchr10:7145514..7270830hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38125317
hg19125317
hg18125317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707681
Samples
Known GenesSFMBT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041863
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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