A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137036



Internal ID18932788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:150084364..150084467hg38UCSC Ensembl
Outerchr5:149463927..149464030hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3974963
SamplesKWS2
Known GenesCSF1R
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137036
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