A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027498



Internal ID19116717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4255406..4471401hg38UCSC Ensembl
Innerchr6:4255640..4471635hg19UCSC Ensembl
Innerchr6:4200639..4416634hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38215996
hg19215996
hg18215996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5911n100
Supporting Variantsnssv3654730, nssv3747903, nssv3747904, nssv3654729, nssv3654728, nssv3654727
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)nsv1027498
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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