A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120308



Internal ID19280745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:25999784..25999858hg38UCSC Ensembl
Outerchr15:26244931..26245005hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961871
SamplesKWS1
Known GenesLOC100128714
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120308
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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