A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115984



Internal ID19252954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:100544304..100544360hg38UCSC Ensembl
Outerchr15:101084509..101084565hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978546
SamplesKWS2
Known GenesCERS3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115984
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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