A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047205



Internal ID18789736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46305526..46333357hg38UCSC Ensembl
Innerchr10:47676762..47704593hg19UCSC Ensembl
Innerchr10:47146768..47174599hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3827832
hg1927832
hg1827832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv847n100
Supporting Variantsnssv3706823
Samples
Known GenesANTXRL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047205
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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