A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046533



Internal ID19135752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123205403..123237626hg38UCSC Ensembl
Innerchr10:124964919..124997142hg19UCSC Ensembl
Innerchr10:124954909..124987132hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3832224
hg1932224
hg1832224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513052
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046533
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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