A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031368



Internal ID19120590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77626179..77793334hg38UCSC Ensembl
Innerchr6:78335896..78503051hg19UCSC Ensembl
Innerchr6:78392615..78559770hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38167156
hg19167156
hg18167156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3659056
Samples
Known GenesMEI4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031368
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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