A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018528



Internal ID19107745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64996668..65190495hg38UCSC Ensembl
Innerchr6:65706561..65900388hg19UCSC Ensembl
Innerchr6:65763282..65957109hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38193828
hg19193828
hg18193828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5998n100
Supporting Variantsnssv3657659
Samples
Known GenesEYS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018528
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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