A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986417



Internal ID18876296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:170020587..170020641hg38UCSC Ensembl
Outerchr4:170941738..170941792hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131843
Supporting Variants
SamplesKWS1
Known GenesMFAP3L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986417
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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