A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027588



Internal ID19116807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77517471..77600338hg38UCSC Ensembl
Innerchr8:78429707..78512574hg19UCSC Ensembl
Innerchr8:78592262..78675129hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3882868
hg1982868
hg1882868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757299
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)nsv1027588
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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