A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022379



Internal ID19111597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80875732..80911578hg38UCSC Ensembl
Innerchr6:81585449..81621295hg19UCSC Ensembl
Innerchr6:81642168..81678014hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3835847
hg1935847
hg1835847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648865, nssv3648866
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)nsv1022379
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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