A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130105



Internal ID18914126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:106535755..106536065hg38UCSC Ensembl
Outerchr6:106983630..106983940hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3358n106
Supporting Variantsnssv3966010
SamplesKWS2
Known GenesAIM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130105
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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