A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014399



Internal ID18756933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121352476..121363980hg38UCSC Ensembl
Innerchr4:122273631..122285135hg19UCSC Ensembl
Innerchr4:122493081..122504585hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3811505
hg1911505
hg1811505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5376n100
Supporting Variantsnssv3639361, nssv3639359, nssv3639360
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)nsv1014399
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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