A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121273



Internal ID19282148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:190237619..190237920hg38UCSC Ensembl
Outerchr3:189955408..189955709hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2658n106
Supporting Variantsnssv3970257, nssv3966775
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121273
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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