A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047412



Internal ID18789943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110987991..111021655hg38UCSC Ensembl
Innerchr10:112747749..112781413hg19UCSC Ensembl
Innerchr10:112737739..112771403hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3833665
hg1933665
hg1833665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518584
Samples
Known GenesSHOC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047412
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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