A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151621



Internal ID18849994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:37187235..37187520hg38UCSC Ensembl
Outerchr20:35815638..35815923hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003041
SamplesKWB1
Known GenesRPN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151621
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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