A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977225



Internal ID19244204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:101901697..101979697hg38UCSC Ensembl
Outerchr15:102441900..102519900hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3878001
hg1978001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139640
Supporting Variants
SamplesKWS2
Known GenesDDX11L9, FAM138E, MIR6859-1, MIR6859-2, OR4F4, WASH3P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977225
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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