A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604764



Internal ID16392173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139283657..139286262hg38UCSC Ensembl
Innerchr6:139604794..139607399hg19UCSC Ensembl
Innerchr6:139646487..139649092hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg382606
hg192606
hg182606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10952n54
Supporting Variantsnssv1073800, nssv1073799
Samples
Known GenesTXLNB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604764
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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