A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3002603



Internal ID16948869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110105993..110106306hg38UCSC Ensembl
Outerchr11:109976718..109977031hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958607
Supporting Variants
SamplesBILGI_BIOE
Known GenesZC3H12C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3002603
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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