A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025069



Internal ID18767601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125973448..126003809hg38UCSC Ensembl
Innerchr6:126294594..126324955hg19UCSC Ensembl
Innerchr6:126336287..126366648hg18UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg3830362
hg1930362
hg1830362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654382
Samples
Known GenesHINT3, TRMT11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025069
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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