A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029292



Internal ID19118511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:29872727..29889225hg38UCSC Ensembl
Innerchr8:29730243..29746741hg19UCSC Ensembl
Innerchr8:29849785..29866283hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3816499
hg1916499
hg1816499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685551
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)nsv1029292
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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