A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121839



Internal ID18938811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67113829..67119729hg38UCSC Ensembl
Outerchr11:66881300..66887200hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385901
hg195901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968491
SamplesKWS2
Known GenesKDM2A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121839
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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