A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008369



Internal ID19097587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38355108..38390275hg38UCSC Ensembl
Innerchr4:38356729..38391896hg19UCSC Ensembl
Innerchr4:38033124..38068291hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3835168
hg1935168
hg1835168
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625031
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)nsv1008369
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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