A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022081



Internal ID18764615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:153399549..153993956hg38UCSC Ensembl
Innerchr4:154320701..154915108hg19UCSC Ensembl
Innerchr4:154540151..155134558hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38594408
hg19594408
hg18594408
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636127
Samples
Known GenesKIAA0922, MND1, RNF175, SFRP2, TLR2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022081
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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