A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138361



Internal ID18921883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43301169..43301230hg38UCSC Ensembl
Outerchr15:43593367..43593428hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3955124, nssv3990924
SamplesKWS2, KWS1
Known GenesTGM7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138361
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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