A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997899



Internal ID17290851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:177902400..177932699hg38UCSC Ensembl
Outerchr5:177329401..177359700hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3830300
hg1930300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950727
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997899
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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