A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128834



Internal ID19264060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63339148..63340748hg38UCSC Ensembl
Outerchr20:61970500..61972100hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2291n106
Supporting Variantsnssv3961502
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128834
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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