A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600997



Internal ID16041720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:14203641..14764752hg38UCSC Ensembl
Innerchr6:14203872..14764983hg19UCSC Ensembl
Innerchr6:14311851..14872962hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38561112
hg19561112
hg18561112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153633
Samples1780862226_A
Known GenesLINC01108
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600997
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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