A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109370



Internal ID18903724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:136268387..136269473hg38UCSC Ensembl
Outerchr6:136589525..136590611hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381087
hg191087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3399n106
Supporting Variantsnssv3956057
SamplesKWS1
Known GenesBCLAF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109370
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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