A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996754



Internal ID16943020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:101345944..101347943hg38UCSC Ensembl
Outerchr4:102267101..102269100hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950367
Supporting Variants
SamplesBILGI_BIOE
Known GenesFLJ20021, PPP3CA
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996754
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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