A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999557



Internal ID16945823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63901229..63928128hg38UCSC Ensembl
Outerchr11:63668701..63695600hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3826900
hg1926900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951009
Supporting Variants
SamplesBILGI_BIOE
Known GenesMARK2, RCOR2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999557
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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