A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040397



Internal ID18782928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6087796..6116734hg38UCSC Ensembl
Innerchr10:6129759..6158697hg19UCSC Ensembl
Innerchr10:6169765..6198703hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3828939
hg1928939
hg1828939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707675
Samples
Known GenesRBM17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040397
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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