A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029189



Internal ID19118408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:57424045..57496729hg38UCSC Ensembl
Innerchr8:58336604..58409288hg19UCSC Ensembl
Innerchr8:58499158..58571842hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3872685
hg1972685
hg1872685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689449
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)nsv1029189
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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