A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999817



Internal ID17292769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:34730496..34734095hg38UCSC Ensembl
Outerchr19:35221401..35225000hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953281
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999817
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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