A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605340



Internal ID16046063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167198269..167370176hg38UCSC Ensembl
Innerchr6:167611757..167783664hg19UCSC Ensembl
Innerchr6:167531747..167703654hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38171908
hg19171908
hg18171908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11056n54
Supporting Variantsnssv1077044
Samples
Known GenesTTLL2, UNC93A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605340
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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