A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999562



Internal ID16945828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:64888129..64917128hg38UCSC Ensembl
Outerchr11:64655601..64684600hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3829000
hg1929000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951014
Supporting Variants
SamplesBILGI_BIOE
Known GenesATG2A, MIR192, MIR194-2, MIR6749, MIR6750
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999562
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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