A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042216



Internal ID19131435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70332807..70368538hg38UCSC Ensembl
Innerchr10:72092563..72128294hg19UCSC Ensembl
Innerchr10:71762569..71798300hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3835732
hg1935732
hg1835732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3506489
Samples
Known GenesLRRC20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042216
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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