A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113708



Internal ID19256688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:48943934..48943999hg38UCSC Ensembl
Outerchr15:49236131..49236196hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969773
SamplesKWS2
Known GenesSHC4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113708
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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