A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031013



Internal ID19120234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55627476..55728664hg38UCSC Ensembl
Innerchr8:56540035..56641223hg19UCSC Ensembl
Innerchr8:56702589..56803777hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38101189
hg19101189
hg18101189
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688677
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)nsv1031013
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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