A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138145



Internal ID19253095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:138045054..138046060hg38UCSC Ensembl
Outerchr4:138966208..138967214hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg381007
hg191007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2910n106
Supporting Variantsnssv3990691
SamplesKWS1
Known GenesLINC00616
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138145
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