A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126485



Internal ID18915266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:58671468..58671868hg38UCSC Ensembl
Outerchr18:56338700..56339100hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984736
SamplesKWS1
Known GenesMALT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126485
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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