A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144744



Internal ID18933677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:90871370..90872070hg38UCSC Ensembl
Outerchr15:91414600..91415300hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981334
SamplesKWS1
Known GenesFURIN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144744
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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