A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005654



Internal ID19094871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43372605..43684173hg38UCSC Ensembl
Innerchr4:43374622..43686190hg19UCSC Ensembl
Innerchr4:43069379..43380947hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38311569
hg19311569
hg18311569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739363
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)nsv1005654
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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