A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115982



Internal ID18931963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:88652238..88652292hg38UCSC Ensembl
Outerchr15:89195469..89195523hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978544
SamplesKWS2
Known GenesISG20
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115982
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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