A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605238



Internal ID16392647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164709839..164800526hg38UCSC Ensembl
Innerchr6:165130872..165214015hg19UCSC Ensembl
Innerchr6:165050862..165134005hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3890688
hg1983144
hg1883144
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11034n54
Supporting Variantsnssv1075794, nssv1075792, nssv1075793, nssv1075795, nssv1075789, nssv1075790, nssv1075791, nssv1154704, nssv1154705
SamplesHGDP00878, HGDP00872
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605238
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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