A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052357



Internal ID18794888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120592928..120710371hg38UCSC Ensembl
Innerchr10:122352440..122469883hg19UCSC Ensembl
Innerchr10:122342430..122459873hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38117444
hg19117444
hg18117444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519186
Samples
Known GenesC10orf85, MIR5694
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052357
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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