A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605463



Internal ID16392872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168316451..168317790hg38UCSC Ensembl
Innerchr6:168717131..168718470hg19UCSC Ensembl
Innerchr6:168459980..168461319hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381340
hg191340
hg181340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11067n54
Supporting Variantsnssv1077304, nssv1077307, nssv1077305, nssv1077303, nssv1077306
Samples
Known GenesDACT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605463
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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