A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024806



Internal ID18767337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10747928..10805045hg38UCSC Ensembl
Innerchr8:10605438..10662555hg19UCSC Ensembl
Innerchr8:10642848..10699965hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3857118
hg1957118
hg1857118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7012n100
Supporting Variantsnssv3754236
Samples
Known GenesPINX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024806
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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