A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997872



Internal ID17290824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:166126396..166136395hg38UCSC Ensembl
Outerchr5:165553401..165563400hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950439
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997872
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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