A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133508



Internal ID19278338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:57525044..57527144hg38UCSC Ensembl
Outerchr20:56100100..56102200hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg382101
hg192101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2272n106
Supporting Variantsnssv3969070
SamplesKWS2
Known GenesCTCFL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133508
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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