A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113545



Internal ID18938194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:20737188..20737258hg38UCSC Ensembl
Outerchr13:21311327..21311397hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968851
SamplesKWS2
Known GenesN6AMT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113545
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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