A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517048



Internal ID15444341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25552710..25581609hg38UCSC Ensembl
Innerchr4:25554332..25583231hg19UCSC Ensembl
Innerchr4:25163430..25192329hg18UCSC Ensembl
Innerchr4:25230601..25259500hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3828900
hg1928900
hg1828900
hg1728900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669906, nssv653687, nssv686406, nssv663156, nssv668055, nssv685272, nssv664880, nssv680823, nssv693040, nssv668997, nssv669890, nssv676616, nssv670403, nssv656102, nssv692411, nssv653003, nssv689543, nssv651871, nssv674058, nssv673930
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517048
Frequency
Sample Size2026
Observed Gain20
Observed Loss0
Observed Complex0
Frequencyn/a


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