A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025276



Internal ID19114494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:55484840..55509380hg38UCSC Ensembl
Innerchr6:55349638..55374178hg19UCSC Ensembl
Innerchr6:55457597..55482137hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3824541
hg1924541
hg1824541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745494
Samples
Known GenesHMGCLL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025276
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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