A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005212



Internal ID16951478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:76027529..76027756hg38UCSC Ensembl
Outerchr4:76948682..76948909hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955670
Supporting Variants
SamplesBILGI_BIOE
Known GenesART3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005212
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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