A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003747



Internal ID18746278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121352476..121369976hg38UCSC Ensembl
Innerchr4:122273631..122291131hg19UCSC Ensembl
Innerchr4:122493081..122510581hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3817501
hg1917501
hg1817501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5377n100
Supporting Variantsnssv3639362
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)nsv1003747
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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