A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986121



Internal ID18873130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:44092592..44092648hg38UCSC Ensembl
Outerchr21:45512473..45512529hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139033
Supporting Variants
SamplesKWS1
Known GenesTRAPPC10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986121
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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