A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009842



Internal ID19099061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3593306..3707900hg38UCSC Ensembl
Innerchr4:3595033..3709627hg19UCSC Ensembl
Innerchr4:3564831..3679425hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38114595
hg19114595
hg18114595
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5083n100
Supporting Variantsnssv3616119
Samples
Known GenesLOC100133461
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009842
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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