A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994144



Internal ID19225707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41573880..41577887hg38UCSC Ensembl
Outerchr15:41866078..41870085hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384008
hg194008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1142657
Supporting Variants
SamplesKWS1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994144
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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