A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144286



Internal ID19262310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:100427118..100427518hg38UCSC Ensembl
Outerchr9:103189400..103189800hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4107n106
Supporting Variantsnssv3995021
SamplesKWS1
Known GenesMSANTD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144286
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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