A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966010



Internal ID18883075
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 StatusS
Merged Variantsnsv1130105
Supporting Variants
SamplesKWS2
Known GenesAIM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966010
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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