A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998139



Internal ID17291091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3351471..3358370hg38UCSC Ensembl
Outerchr11:3372701..3379600hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951297
Supporting Variants
SamplesBILGI_BIOE
Known GenesZNF195
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998139
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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