A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109774



Internal ID18917436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:46564088..46564186hg38UCSC Ensembl
Outerchr6:46531825..46531923hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958125
SamplesKWS1
Known GenesCYP39A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109774
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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