A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022609



Internal ID19111827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13313102..13381369hg38UCSC Ensembl
Innerchr8:13170611..13238878hg19UCSC Ensembl
Innerchr8:13214982..13283249hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3868268
hg1968268
hg1868268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3666988, nssv3666989
Samples
Known GenesDLC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022609
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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