A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955764



Internal ID16957951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:44794892..44795447hg38UCSC Ensembl
Outerchr5:44794994..44795549hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv162n73
Supporting Variantsnssv3002055
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955764
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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