A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998938



Internal ID16945204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:7669315..7700414hg38UCSC Ensembl
Outerchr19:7734201..7765300hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3831100
hg1931100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953959
Supporting Variants
SamplesBILGI_BIOE
Known GenesC19orf59, FCER2, RETN, TRAPPC5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998938
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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