A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126077



Internal ID18929416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41562774..41565038hg38UCSC Ensembl
Outerchr15:41854972..41857236hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382265
hg192265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984285
SamplesKWS1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126077
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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