A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003707



Internal ID19092925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19897260..19961590hg38UCSC Ensembl
Innerchr4:19898883..19963213hg19UCSC Ensembl
Innerchr4:19507981..19572311hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3864331
hg1964331
hg1864331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619881
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)nsv1003707
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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