A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016339



Internal ID19105558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94543826..94573579hg38UCSC Ensembl
Innerchr8:95556054..95585807hg19UCSC Ensembl
Innerchr8:95625230..95654983hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3829754
hg1929754
hg1829754
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7273n100
Supporting Variantsnssv3689730
Samples
Known GenesKIAA1429
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016339
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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