A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994769



Internal ID18868792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184314312..184315112hg38UCSC Ensembl
Outerchr3:184032100..184032900hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144053
Supporting Variants
SamplesKWS1
Known GenesEIF4G1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994769
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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