A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018622



Internal ID18761155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:55433056..55455513hg38UCSC Ensembl
Innerchr6:55297854..55320311hg19UCSC Ensembl
Innerchr6:55405813..55428270hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3822458
hg1922458
hg1822458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657494
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)nsv1018622
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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