A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3002926



Internal ID17295878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:58410579..58410778hg38UCSC Ensembl
Outerchr19:58921946..58922145hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954672
Supporting Variants
SamplesBILGI_BIOE
Known GenesZNF584
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3002926
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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