A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111836



Internal ID18911292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69123184..69128484hg38UCSC Ensembl
Outerchr9:71738100..71743400hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385301
hg195301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4064n106
Supporting Variantsnssv3964746
SamplesKWS2
Known GenesTJP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111836
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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