A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145362



Internal ID18930350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:45108700..45108787hg38UCSC Ensembl
Outerchr21:46528615..46528702hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2407n106
Supporting Variantsnssv3982474
SamplesKWS1
Known GenesADARB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145362
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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