A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005009



Internal ID16951275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:74821314..74821695hg38UCSC Ensembl
Outerchr11:74532359..74532740hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv957195
Supporting Variants
SamplesBILGI_BIOE
Known GenesRNF169
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005009
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