A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014710



Internal ID18757245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121352476..121370988hg38UCSC Ensembl
Innerchr4:122273631..122292143hg19UCSC Ensembl
Innerchr4:122493081..122511593hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3818513
hg1918513
hg1818513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5377n100
Supporting Variantsnssv3639363
Samples
Known GenesQRFPR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014710
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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