A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999796



Internal ID17292748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:24253499..24447898hg38UCSC Ensembl
Outerchr19:24436301..24630700hg19UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38194400
hg19194400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953260
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999796
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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