A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048029



Internal ID18790560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:63414026..63565535hg38UCSC Ensembl
Innerchr15:63706225..63857734hg19UCSC Ensembl
Innerchr15:61493278..61644787hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38151510
hg19151510
hg18151510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553646
Samples
Known GenesUSP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048029
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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