A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006049



Internal ID19095267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29573050..29599188hg38UCSC Ensembl
Innerchr4:29574672..29600810hg19UCSC Ensembl
Innerchr4:29183770..29209908hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3826139
hg1926139
hg1826139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620636
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)nsv1006049
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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