A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024977



Internal ID19114195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:21451079..21733222hg38UCSC Ensembl
Innerchr5:21451188..21733331hg19UCSC Ensembl
Innerchr5:21486945..21769088hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38282144
hg19282144
hg18282144
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5605n100
Supporting Variantsnssv3635937
Samples
Known GenesGUSBP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024977
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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