A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041904



Internal ID19131123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7906899..7952921hg38UCSC Ensembl
Innerchr10:7948862..7994884hg19UCSC Ensembl
Innerchr10:7988868..8034890hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3846023
hg1946023
hg1846023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3491677
Samples
Known GenesTAF3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041904
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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