A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989734



Internal ID19227538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63768328..63768728hg38UCSC Ensembl
Outerchr11:63535800..63536200hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136128
Supporting Variants
SamplesKWS2
Known GenesC11orf95
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989734
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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