A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986232



Internal ID18860566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:99832623..99832693hg38UCSC Ensembl
Outerchr3:99551467..99551537hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131715
Supporting Variants
SamplesKWS1
Known GenesCMSS1, MIR548G
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986232
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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