A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046262



Internal ID18788793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77154478..77173657hg38UCSC Ensembl
Innerchr9:79769394..79788573hg19UCSC Ensembl
Innerchr9:78959214..78978393hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3819180
hg1919180
hg1819180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7682n100
Supporting Variantsnssv3696377
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046262
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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