A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022434



Internal ID19111652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11008732..11059013hg38UCSC Ensembl
Innerchr8:10866242..10916523hg19UCSC Ensembl
Innerchr8:10903652..10953933hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3850282
hg1950282
hg1850282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681728
Samples
Known GenesMIR598, XKR6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022434
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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