A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610007



Internal ID16050730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6797870..6971563hg38UCSC Ensembl
Innerchr8:6655391..6829085hg19UCSC Ensembl
Innerchr8:6642801..6816495hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38173694
hg19173695
hg18173695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156822
SamplesHGDP00805
Known GenesDEFA10P, DEFA4, DEFA6, DEFA8P, DEFA9P, DEFB1, LOC100652791, XKR5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610007
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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