A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998246



Internal ID18811096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92277694..92429174hg38UCSC Ensembl
Innerchr4:93198845..93350325hg19UCSC Ensembl
Innerchr4:93417868..93569348hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38151481
hg19151481
hg18151481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3630965
Samples
Known GenesGRID2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998246
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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