A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604763



Internal ID16392172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139283657..139285949hg38UCSC Ensembl
Innerchr6:139604794..139607086hg19UCSC Ensembl
Innerchr6:139646487..139648779hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg382293
hg192293
hg182293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10952n54
Supporting Variantsnssv1073795, nssv1073796, nssv1073793, nssv1073798, nssv1073797, nssv1073794
Samples
Known GenesTXLNB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604763
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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