A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029008



Internal ID19118227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25660633..25737704hg38UCSC Ensembl
Innerchr8:25518149..25595220hg19UCSC Ensembl
Innerchr8:25574066..25651137hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3877072
hg1977072
hg1877072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7150n100
Supporting Variantsnssv3685510
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)nsv1029008
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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