A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999570



Internal ID16945836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67493430..67504729hg38UCSC Ensembl
Outerchr11:67260901..67272200hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3811300
hg1911300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951022
Supporting Variants
SamplesBILGI_BIOE
Known GenesPITPNM1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999570
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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