A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041698



Internal ID18784229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70244698..70306282hg38UCSC Ensembl
Innerchr10:72004454..72066038hg19UCSC Ensembl
Innerchr10:71674460..71736044hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3861585
hg1961585
hg1861585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513337
Samples
Known GenesLRRC20, NPFFR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041698
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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