A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001565



Internal ID18744096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180167906..180201389hg38UCSC Ensembl
Innerchr1:180137041..180170524hg19UCSC Ensembl
Innerchr1:178403664..178437147hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3833484
hg1933484
hg1833484
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3500891
Samples
Known GenesFLJ23867, QSOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001565
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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