A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027287



Internal ID19116506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66511029..67587333hg38UCSC Ensembl
Innerchr6:67220922..68297226hg19UCSC Ensembl
Innerchr6:67277643..68353947hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381076305
hg191076305
hg181076305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658756
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)nsv1027287
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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