A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111664



Internal ID19275006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:3499139..3499477hg38UCSC Ensembl
Outerchr5:3499253..3499591hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3028n106
Supporting Variantsnssv3964561
SamplesKWS2
Known GenesLINC01019, LOC102467075
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111664
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer