A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513337



Internal ID18464932
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 StatusS
Merged Variantsnsv1041698
Supporting Variants
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)nssv3513337
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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