A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119257



Internal ID18901488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12380193..12380812hg38UCSC Ensembl
Outerchr11:12401740..12402359hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv589n106
Supporting Variantsnssv3959693
SamplesKWS1
Known GenesPARVA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119257
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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