A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604526



Internal ID16391935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:113380747..113381782hg38UCSC Ensembl
Innerchr6:113701949..113702984hg19UCSC Ensembl
Innerchr6:113808642..113809677hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381036
hg191036
hg181036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10913n54
Supporting Variantsnssv1072085, nssv1072084, nssv1072083
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604526
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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