A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020982



Internal ID19110200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:72327312..72410855hg38UCSC Ensembl
Innerchr8:73239547..73323090hg19UCSC Ensembl
Innerchr8:73402101..73485644hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3883544
hg1983544
hg1883544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689527, nssv3689526
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)nsv1020982
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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