A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025722



Internal ID19114939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50159790..50265382hg38UCSC Ensembl
Innerchr5:49455624..49561216hg19UCSC Ensembl
Innerchr5:49491381..49596973hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38105593
hg19105593
hg18105593
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5663n100
Supporting Variantsnssv3642101, nssv3642100
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)nsv1025722
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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