A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526977



Internal ID15454270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57273804..57738815hg38UCSC Ensembl
Innerchr4:58139970..58604981hg19UCSC Ensembl
Innerchr4:57834727..58299738hg18UCSC Ensembl
Innerchr4:57980898..58445909hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38465012
hg19465012
hg18465012
hg17465012
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv320n21
Supporting Variantsnssv703349
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526977
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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