A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027744



Internal ID19116962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88514342..88597422hg38UCSC Ensembl
Innerchr8:89526571..89609651hg19UCSC Ensembl
Innerchr8:89595687..89678767hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3883081
hg1983081
hg1883081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689689
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)nsv1027744
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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