A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021119



Internal ID19110337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:30305736..30336463hg38UCSC Ensembl
Innerchr8:30163252..30193979hg19UCSC Ensembl
Innerchr8:30282794..30313521hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3830728
hg1930728
hg1830728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685553
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)nsv1021119
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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