A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023825



Internal ID18766358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:51756264..51803577hg38UCSC Ensembl
Innerchr8:52668824..52716137hg19UCSC Ensembl
Innerchr8:52831377..52878690hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3847314
hg1947314
hg1847314
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757257
Samples
Known GenesPXDNL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023825
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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