A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971933



Internal ID18897135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43453966..43454034hg38UCSC Ensembl
Outerchr15:43746164..43746232hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134438
Supporting Variants
SamplesKWS2
Known GenesRNU6-28P, TP53BP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971933
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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