A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999838



Internal ID16946104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39320661..39330060hg38UCSC Ensembl
Outerchr19:39811301..39820700hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953572
Supporting Variants
SamplesBILGI_BIOE
Known GenesGMFG
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999838
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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