A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029150



Internal ID19118369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25660633..25730114hg38UCSC Ensembl
Innerchr8:25518149..25587630hg19UCSC Ensembl
Innerchr8:25574066..25643547hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3869482
hg1969482
hg1869482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7150n100
Supporting Variantsnssv3685509, nssv3760498, nssv3760497
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)nsv1029150
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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