A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109652



Internal ID18911589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:168155409..168155536hg38UCSC Ensembl
Outerchr4:169076560..169076687hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957191
SamplesKWS1
Known GenesANXA10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109652
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