A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3973987



Internal ID18887090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:101320426..101320492hg38UCSC Ensembl
Outerchr4:102241583..102241649hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123824
Supporting Variants
SamplesKWS2
Known GenesPPP3CA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3973987
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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