A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951297



Internal ID17300171
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 StatusM
Merged Variants
Supporting Variantsnssv2998139
SamplesBILGI_BIOE
Known GenesZNF195
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951297
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer