A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025400



Internal ID19114618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:54685803..54818156hg38UCSC Ensembl
Innerchr8:55598363..55730716hg19UCSC Ensembl
Innerchr8:55760917..55893270hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38132354
hg19132354
hg18132354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3688674
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)nsv1025400
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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