A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998922



Internal ID16945188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:2169602..2236001hg38UCSC Ensembl
Outerchr19:2169601..2236000hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3866400
hg1966400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953943
Supporting Variants
SamplesBILGI_BIOE
Known GenesDOT1L, MIR1227, MIR6789, PLEKHJ1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998922
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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