A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3991904



Internal ID18899574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:88942606..88942662hg38UCSC Ensembl
Outerchr4:89863757..89863813hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139282
Supporting Variants
SamplesKWS2
Known GenesFAM13A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3991904
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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