A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113705



Internal ID19284589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41571686..41572441hg38UCSC Ensembl
Outerchr15:41863884..41864639hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954749, nssv3990921
SamplesKWS2, KWS1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113705
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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