A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049576



Internal ID18792107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50452584..50551298hg38UCSC Ensembl
Innerchr15:50744781..50843495hg19UCSC Ensembl
Innerchr15:48532073..48630787hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3898715
hg1998715
hg1898715
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552387
Samples
Known GenesUSP50, USP8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049576
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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