A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031726



Internal ID18774260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10770232..10891859hg38UCSC Ensembl
Innerchr8:10627742..10749369hg19UCSC Ensembl
Innerchr8:10665152..10786779hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38121628
hg19121628
hg18121628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3754237
Samples
Known GenesMIR1322, PINX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031726
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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