A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028764



Internal ID19117982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76161254..76435856hg38UCSC Ensembl
Innerchr6:76870971..77145573hg19UCSC Ensembl
Innerchr6:76927691..77202293hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38274603
hg19274603
hg18274603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658820
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)nsv1028764
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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