A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109368



Internal ID18932417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:136261531..136268225hg38UCSC Ensembl
Outerchr6:136582669..136589363hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg386695
hg196695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3398n106
Supporting Variantsnssv3956055
SamplesKWS1
Known GenesBCLAF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109368
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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