A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156499



Internal ID22086900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41650440..41652999hg38UCSC Ensembl
Outerchr6:41647191..41657691hg38UCSC Ensembl
Innerchr6:41618178..41620737hg19UCSC Ensembl
Outerchr6:41614929..41625429hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3810501
hg1910501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018556
Samples
Known GenesMDFI
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156499
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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