A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965916



Internal ID19242095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:161527758..161609344hg38UCSC Ensembl
Outerchr1:161497548..161579134hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3881587
hg1981587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112219
Supporting Variants
SamplesKWS2
Known GenesFCGR2C, FCGR3A, HSPA7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965916
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