A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997789



Internal ID17290741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:88141384..88141983hg38UCSC Ensembl
Outerchr5:87437201..87437800hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950100
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997789
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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