A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126922



Internal ID18927829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:37187223..37187519hg38UCSC Ensembl
Outerchr20:35815626..35815922hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2248n106
Supporting Variantsnssv3985201
SamplesKWS1
Known GenesRPN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126922
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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