A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053079



Internal ID19142298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78824844..78859088hg38UCSC Ensembl
Innerchr9:81439760..81474004hg19UCSC Ensembl
Innerchr9:80629580..80663824hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3834245
hg1934245
hg1834245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7684n100
Supporting Variantsnssv3697512
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)nsv1053079
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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