A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007392



Internal ID19096611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121409652..121479295hg38UCSC Ensembl
Innerchr4:122330807..122400450hg19UCSC Ensembl
Innerchr4:122550257..122619900hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3869644
hg1969644
hg1869644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5379n100
Supporting Variantsnssv3639381
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007392
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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