A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025575



Internal ID19114793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:58697266..58719576hg38UCSC Ensembl
Innerchr8:59609825..59632135hg19UCSC Ensembl
Innerchr8:59772379..59794689hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3822311
hg1922311
hg1822311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757280
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025575
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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