A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010691



Internal ID19099908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:168589163..168630432hg38UCSC Ensembl
Innerchr3:168306951..168348220hg19UCSC Ensembl
Innerchr3:169789645..169830914hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3841270
hg1941270
hg1841270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3612699
Samples
Known GenesEGFEM1P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010691
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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