A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064807



Internal ID18807338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9695359..9770361hg38UCSC Ensembl
Innerchr18:9695356..9770358hg19UCSC Ensembl
Innerchr18:9685356..9760358hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3875003
hg1975003
hg1875003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564098
Samples
Known GenesRAB31
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064807
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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