A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974662



Internal ID18891371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:115820035..115820101hg38UCSC Ensembl
Outerchr3:115538882..115538948hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136765
Supporting Variants
SamplesKWS2
Known GenesLSAMP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974662
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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