A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020205



Internal ID19109424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4255406..4473880hg38UCSC Ensembl
Innerchr6:4255640..4474114hg19UCSC Ensembl
Innerchr6:4200639..4419113hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38218475
hg19218475
hg18218475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5911n100
Supporting Variantsnssv3654731
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)nsv1020205
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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