A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997898



Internal ID18810748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:92701571..92762599hg38UCSC Ensembl
Innerchr1:93167128..93228156hg19UCSC Ensembl
Innerchr1:92939716..93000744hg18UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3861029
hg1961029
hg1861029
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3464574
Samples
Known GenesEVI5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997898
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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