A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999807



Internal ID16946073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:30222894..30229493hg38UCSC Ensembl
Outerchr19:30713801..30720400hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953271
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999807
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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