A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024637



Internal ID18767169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18994017..19008731hg38UCSC Ensembl
Innerchr8:18851527..18866241hg19UCSC Ensembl
Innerchr8:18895807..18910521hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3814715
hg1914715
hg1814715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7128n100
Supporting Variantsnssv3684211, nssv3684210, nssv3684209
Samples
Known GenesPSD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024637
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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