A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125877



Internal ID18923075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:46577010..46577115hg38UCSC Ensembl
Outerchr20:45205649..45205754hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2258n106
Supporting Variantsnssv3984084
SamplesKWS1
Known GenesSLC13A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125877
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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