A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026694



Internal ID18769225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:38214790..38249049hg38UCSC Ensembl
Innerchr8:38072308..38106567hg19UCSC Ensembl
Innerchr8:38191465..38225724hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3834260
hg1934260
hg1834260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7165n100
Supporting Variantsnssv3685585
Samples
Known GenesDDHD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026694
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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