A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3681727



Internal ID18633322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10753035..10800216hg38UCSC Ensembl
Innerchr8:10610545..10657726hg19UCSC Ensembl
Innerchr8:10647955..10695136hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3847182
hg1947182
hg1847182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031709
Supporting Variants
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)nssv3681727
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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