A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113690



Internal ID19258796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:22988141..22990717hg38UCSC Ensembl
Outerchr15:22882351..22884927hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382577
hg192577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969007, nssv3970946
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113690
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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