A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112898



Internal ID18905928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:28510223..28623423hg38UCSC Ensembl
Outerchr6:28478000..28591200hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38113201
hg19113201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3296n106
Supporting Variantsnssv3967398
SamplesKWS2
Known GenesGPX5, GPX6, SCAND3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112898
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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