A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999631



Internal ID16945897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:119308591..119317490hg38UCSC Ensembl
Outerchr11:119179301..119188200hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952747
Supporting Variants
SamplesBILGI_BIOE
Known GenesMCAM, MIR6756
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999631
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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