A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003671



Internal ID18746202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:54579485..54647108hg38UCSC Ensembl
Innerchr4:55445652..55513275hg19UCSC Ensembl
Innerchr4:55140409..55208032hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3867624
hg1967624
hg1867624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5210n100
Supporting Variantsnssv3625275
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)nsv1003671
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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